Canonical Allele Identifier: CA453644063

Gene: PMS2

Linked Data

• dbSNP Id: rs1583334058
• MyVariant Identifiers: chr7:g.6029446G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5989815G>A , CM000669.2:g.5989815G>A	GRCh38
NC_000007.13:g.6029446G>A , CM000669.1:g.6029446G>A	GRCh37
NC_000007.12:g.5995972G>A	NCBI36
NG_008466.1:g.24292C>T , LRG_161:g.24292C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699814.2:c.*525C>T	ENSP00000514615.2:n.*525C>T
ENST00000699840.2:c.1126C>T	ENSP00000514638.2:p.Leu376=
ENST00000699930.2:c.1021C>T	ENSP00000514695.2:p.Leu341=
ENST00000406569.8:c.1129C>T	ENSP00000514464.1:p.Leu377=
ENST00000644110.2:c.*723C>T	ENSP00000496392.2:n.*723C>T
ENST00000699752.1:c.988+2158C>T	ENSP00000514561.1:n.988+2158C>T
ENST00000699753.1:c.*550C>T	ENSP00000514562.1:n.*550C>T
ENST00000699754.1:c.931C>T	ENSP00000514563.1:p.Leu311=
ENST00000699755.1:c.*528C>T	ENSP00000514564.1:n.*528C>T
ENST00000699756.1:c.*716C>T	ENSP00000514565.1:n.*716C>T
ENST00000699757.1:c.*386C>T	ENSP00000514566.1:n.*386C>T
ENST00000699758.1:c.*386C>T	ENSP00000514567.1:n.*386C>T
ENST00000699759.1:n.1983C>T
ENST00000699760.1:c.811C>T	ENSP00000514568.1:p.Leu271=
ENST00000699761.1:c.724C>T	ENSP00000514569.1:p.Leu242=
ENST00000699762.1:c.556C>T	ENSP00000514570.1:p.Leu186=
ENST00000699763.1:c.*219C>T	ENSP00000514571.1:n.*219C>T
ENST00000699764.1:c.1129C>T	ENSP00000514572.1:p.Leu377=
ENST00000699765.1:c.*225C>T	ENSP00000514573.1:n.*225C>T
ENST00000699766.1:c.1129C>T	ENSP00000514574.1:p.Leu377=
ENST00000699767.1:c.1129C>T	ENSP00000514575.1:p.Leu377=
ENST00000699768.1:c.1129C>T	ENSP00000514576.1:p.Leu377=
ENST00000699811.1:c.724C>T	ENSP00000514614.1:p.Leu242=
ENST00000699813.1:n.1242C>T
ENST00000699814.1:c.752C>T
ENST00000699815.1:c.*621C>T	ENSP00000514616.1:n.*621C>T
ENST00000699816.1:c.724C>T	ENSP00000514617.1:p.Leu242=
ENST00000699817.1:c.*723C>T	ENSP00000514618.1:n.*723C>T
ENST00000699818.1:c.724C>T	ENSP00000514619.1:p.Leu242=
ENST00000699819.1:c.*286C>T	ENSP00000514620.1:n.*286C>T
ENST00000699820.1:c.1129C>T	ENSP00000514621.1:p.Leu377=
ENST00000699821.1:c.724C>T	ENSP00000514622.1:p.Leu242=
ENST00000699822.1:c.*581C>T	ENSP00000514623.1:n.*581C>T
ENST00000699823.1:c.724C>T	ENSP00000514624.1:p.Leu242=
ENST00000699824.1:c.*632C>T	ENSP00000514625.1:n.*632C>T
ENST00000699825.1:c.583+2158C>T	ENSP00000514626.1:n.583+2158C>T
ENST00000699826.1:c.*528C>T	ENSP00000514627.1:n.*528C>T
ENST00000699827.1:c.961C>T	ENSP00000514628.1:p.Leu321=
ENST00000699828.1:c.*219C>T	ENSP00000514629.1:n.*219C>T
ENST00000699829.1:c.*630C>T	ENSP00000514630.1:n.*630C>T
ENST00000699830.1:c.*528C>T	ENSP00000514631.1:n.*528C>T
ENST00000699833.1:n.2901C>T
ENST00000699837.1:c.724C>T	ENSP00000514635.1:p.Leu242=
ENST00000699838.1:c.*1029C>T	ENSP00000514636.1:n.*1029C>T
ENST00000699839.1:c.1315C>T	ENSP00000514637.1:p.Leu439=
ENST00000699840.1:c.1126C>T	ENSP00000514638.1:p.Leu376=
ENST00000699916.1:c.*386C>T	ENSP00000514684.1:n.*386C>T
ENST00000699917.1:c.*578C>T	ENSP00000514685.1:n.*578C>T
ENST00000699918.1:c.*630C>T	ENSP00000514686.1:n.*630C>T
ENST00000699919.1:c.*716C>T	ENSP00000514687.1:n.*716C>T
ENST00000699920.1:c.*765C>T	ENSP00000514688.1:n.*765C>T
ENST00000699928.1:c.988+2158C>T	ENSP00000514693.1:n.988+2158C>T
ENST00000699929.1:c.*430C>T	ENSP00000514694.1:n.*430C>T
ENST00000699930.1:c.1021C>T	ENSP00000514695.1:p.Leu341=
ENST00000699931.1:n.2557C>T
ENST00000699932.1:c.*347C>T	ENSP00000514696.1:n.*347C>T
ENST00000699933.1:n.1109C>T
ENST00000699951.1:c.*225C>T	ENSP00000514706.1:n.*225C>T
ENST00000699952.1:c.803+7511C>T	ENSP00000514707.1:n.803+7511C>T
ENST00000699953.1:c.*236C>T	ENSP00000514708.1:n.*236C>T
ENST00000699954.1:c.*430C>T	ENSP00000514709.1:n.*430C>T
ENST00000265849.12:c.1129C>T MANE Select	ENSP00000265849.7:p.Leu377=
ENST00000642292.1:c.724C>T	ENSP00000495524.1:p.Leu242=
ENST00000642456.1:c.724C>T	ENSP00000493814.1:p.Leu242=
ENST00000643595.1:c.*528C>T	ENSP00000494497.1:n.*528C>T
ENST00000644110.1:c.811C>T	ENSP00000496392.1:p.Leu271=
ENST00000265849.11:c.1129C>T	ENSP00000265849.7:p.Leu377=
ENST00000382321.5:c.804-6824C>T	ENSP00000371758.4:n.804-6824C>T
ENST00000406569.7:n.1129C>T
ENST00000441476.6:c.811C>T	ENSP00000392843.2:p.Leu271=
ENST00000469652.1:n.63-6910C>T
NM_000535.5:c.1129C>T , LRG_161t1:c.1129C>T	NP_000526.1:p.Leu377=
NR_003085.2:n.1211C>T
XM_006715742.2:c.1123C>T	XP_006715805.1:p.Leu375=
XM_006715744.2:c.196C>T	XP_006715807.1:p.Leu66=
XM_011515427.1:c.1174C>T	XP_011513729.1:p.Leu392=
XM_011515428.1:c.1033+2158C>T	XP_011513730.1:n.1033+2158C>T
XM_011515429.1:c.811C>T	XP_011513731.1:p.Leu271=
XM_011515430.1:c.811C>T	XP_011513732.1:p.Leu271=
NM_000535.6:c.1129C>T	NP_000526.2:p.Leu377=
NM_001322003.1:c.724C>T	NP_001308932.1:p.Leu242=
NM_001322004.1:c.724C>T	NP_001308933.1:p.Leu242=
NM_001322005.1:c.724C>T	NP_001308934.1:p.Leu242=
NM_001322006.1:c.988+2158C>T	NP_001308935.1:n.988+2158C>T
NM_001322007.1:c.811C>T	NP_001308936.1:p.Leu271=
NM_001322008.1:c.811C>T	NP_001308937.1:p.Leu271=
NM_001322009.1:c.724C>T	NP_001308938.1:p.Leu242=
NM_001322010.1:c.583+2158C>T	NP_001308939.1:n.583+2158C>T
NM_001322011.1:c.196C>T	NP_001308940.1:p.Leu66=
NM_001322012.1:c.196C>T	NP_001308941.1:p.Leu66=
NM_001322013.1:c.556C>T	NP_001308942.1:p.Leu186=
NM_001322014.1:c.1129C>T	NP_001308943.1:p.Leu377=
NM_001322015.1:c.820C>T	NP_001308944.1:p.Leu274=
NR_136154.1:n.1216C>T
XM_006715744.4:c.196C>T	XP_006715807.1:p.Leu66=
XM_017012342.2:c.196C>T	XP_016867831.1:p.Leu66=
XM_024446800.1:c.583+2158C>T	XP_024302568.1:n.583+2158C>T
NM_000535.7:c.1129C>T MANE Select	NP_000526.2:p.Leu377=
NM_001322003.2:c.724C>T	NP_001308932.1:p.Leu242=
NM_001322004.2:c.724C>T	NP_001308933.1:p.Leu242=
NM_001322005.2:c.724C>T	NP_001308934.1:p.Leu242=
NM_001322006.2:c.988+2158C>T	NP_001308935.1:n.988+2158C>T
NM_001322008.2:c.811C>T	NP_001308937.1:p.Leu271=
NM_001322009.2:c.724C>T	NP_001308938.1:p.Leu242=
NM_001322010.2:c.583+2158C>T	NP_001308939.1:n.583+2158C>T
NM_001322011.2:c.196C>T	NP_001308940.1:p.Leu66=
NM_001322012.2:c.196C>T	NP_001308941.1:p.Leu66=
NM_001322013.2:c.556C>T	NP_001308942.1:p.Leu186=
NM_001322014.2:c.1129C>T	NP_001308943.1:p.Leu377=
NM_001322015.2:c.820C>T	NP_001308944.1:p.Leu274=
NM_001322007.2:c.811C>T	NP_001308936.1:p.Leu271=