Canonical Allele Identifier: CA453646916

Gene: PMS2

Linked Data

• dbSNP Id: rs1210294498
• MyVariant Identifiers: chr7:g.6038805A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5999174A>T , CM000669.2:g.5999174A>T	GRCh38
NC_000007.13:g.6038805A>T , CM000669.1:g.6038805A>T	GRCh37
NC_000007.12:g.6005331A>T	NCBI36
NG_008466.1:g.14933T>A , LRG_161:g.14933T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000699814.2:c.*233T>A	ENSP00000514615.2:n.*233T>A
ENST00000699840.2:c.636T>A	ENSP00000514638.2:p.Pro212=
ENST00000699930.2:c.597+42T>A	ENSP00000514695.2:n.597+42T>A
ENST00000406569.8:c.639T>A	ENSP00000514464.1:p.Pro213=
ENST00000644110.2:c.*233T>A	ENSP00000496392.2:n.*233T>A
ENST00000699752.1:c.639T>A	ENSP00000514561.1:p.Pro213=
ENST00000699753.1:c.*38T>A	ENSP00000514562.1:n.*38T>A
ENST00000699754.1:c.639T>A	ENSP00000514563.1:p.Pro213=
ENST00000699755.1:c.*38T>A	ENSP00000514564.1:n.*38T>A
ENST00000699756.1:c.*226T>A	ENSP00000514565.1:n.*226T>A
ENST00000699757.1:c.88T>A	ENSP00000514566.1:p.Cys30Ser
ENST00000699758.1:c.352T>A	ENSP00000514567.1:p.Cys118Ser
ENST00000699759.1:n.711T>A
ENST00000699760.1:c.321T>A	ENSP00000514568.1:p.Pro107=
ENST00000699761.1:c.234T>A	ENSP00000514569.1:p.Pro78=
ENST00000699762.1:c.133-1751T>A	ENSP00000514570.1:n.133-1751T>A
ENST00000699763.1:c.234T>A	ENSP00000514571.1:p.Pro78=
ENST00000699764.1:c.639T>A	ENSP00000514572.1:p.Pro213=
ENST00000699765.1:c.321T>A	ENSP00000514573.1:p.Pro107=
ENST00000699766.1:c.639T>A	ENSP00000514574.1:p.Pro213=
ENST00000699767.1:c.639T>A	ENSP00000514575.1:p.Pro213=
ENST00000699768.1:c.639T>A	ENSP00000514576.1:p.Pro213=
ENST00000699811.1:c.234T>A	ENSP00000514614.1:p.Pro78=
ENST00000699813.1:n.752T>A
ENST00000699814.1:c.460T>A
ENST00000699815.1:c.*140T>A	ENSP00000514616.1:n.*140T>A
ENST00000699816.1:c.234T>A	ENSP00000514617.1:p.Pro78=
ENST00000699817.1:c.*233T>A	ENSP00000514618.1:n.*233T>A
ENST00000699818.1:c.234T>A	ENSP00000514619.1:p.Pro78=
ENST00000699819.1:c.172T>A	ENSP00000514620.1:p.Cys58Ser
ENST00000699820.1:c.639T>A	ENSP00000514621.1:p.Pro213=
ENST00000699821.1:c.234T>A	ENSP00000514622.1:p.Pro78=
ENST00000699822.1:c.*91T>A	ENSP00000514623.1:n.*91T>A
ENST00000699823.1:c.234T>A	ENSP00000514624.1:p.Pro78=
ENST00000699824.1:c.*142T>A	ENSP00000514625.1:n.*142T>A
ENST00000699825.1:c.234T>A	ENSP00000514626.1:p.Pro78=
ENST00000699826.1:c.*38T>A	ENSP00000514627.1:n.*38T>A
ENST00000699827.1:c.538-1751T>A	ENSP00000514628.1:n.538-1751T>A
ENST00000699828.1:c.639T>A	ENSP00000514629.1:p.Pro213=
ENST00000699829.1:c.*140T>A	ENSP00000514630.1:n.*140T>A
ENST00000699830.1:c.*38T>A	ENSP00000514631.1:n.*38T>A
ENST00000699831.1:n.551T>A
ENST00000699832.1:n.922T>A
ENST00000699833.1:n.719T>A
ENST00000699834.1:n.807+38T>A
ENST00000699837.1:c.234T>A	ENSP00000514635.1:p.Pro78=
ENST00000699838.1:c.*539T>A	ENSP00000514636.1:n.*539T>A
ENST00000699839.1:c.825T>A	ENSP00000514637.1:p.Pro275=
ENST00000699840.1:c.636T>A	ENSP00000514638.1:p.Pro212=
ENST00000699916.1:c.187T>A	ENSP00000514684.1:p.Cys63Ser
ENST00000699917.1:c.*88T>A	ENSP00000514685.1:n.*88T>A
ENST00000699918.1:c.*140T>A	ENSP00000514686.1:n.*140T>A
ENST00000699919.1:c.*226T>A	ENSP00000514687.1:n.*226T>A
ENST00000699920.1:c.*275T>A	ENSP00000514688.1:n.*275T>A
ENST00000699928.1:c.639T>A	ENSP00000514693.1:p.Pro213=
ENST00000699929.1:c.*38T>A	ENSP00000514694.1:n.*38T>A
ENST00000699930.1:c.597+42T>A	ENSP00000514695.1:n.597+42T>A
ENST00000699931.1:n.750T>A
ENST00000699932.1:c.639T>A	ENSP00000514696.1:p.Pro213=
ENST00000699933.1:n.719T>A
ENST00000699951.1:c.639T>A	ENSP00000514706.1:p.Pro213=
ENST00000699952.1:c.639T>A	ENSP00000514707.1:p.Pro213=
ENST00000699953.1:c.639T>A	ENSP00000514708.1:p.Pro213=
ENST00000699954.1:c.*38T>A	ENSP00000514709.1:n.*38T>A
ENST00000265849.12:c.639T>A MANE Select	ENSP00000265849.7:p.Pro213=
ENST00000642292.1:c.234T>A	ENSP00000495524.1:p.Pro78=
ENST00000642456.1:c.234T>A	ENSP00000493814.1:p.Pro78=
ENST00000643595.1:c.*38T>A	ENSP00000494497.1:n.*38T>A
ENST00000644110.1:c.321T>A	ENSP00000496392.1:p.Pro107=
ENST00000265849.11:c.639T>A	ENSP00000265849.7:p.Pro213=
ENST00000382321.5:c.639T>A	ENSP00000371758.4:p.Pro213=
ENST00000406569.7:n.639T>A
ENST00000441476.6:c.321T>A	ENSP00000392843.2:p.Pro107=
ENST00000469652.1:n.62+6819T>A
NM_000535.5:c.639T>A , LRG_161t1:c.639T>A	NP_000526.1:p.Pro213=
NR_003085.2:n.721T>A
XM_006715742.2:c.633T>A	XP_006715805.1:p.Pro211=
XM_011515427.1:c.684T>A	XP_011513729.1:p.Pro228=
XM_011515428.1:c.684T>A	XP_011513730.1:p.Pro228=
XM_011515429.1:c.321T>A	XP_011513731.1:p.Pro107=
XM_011515430.1:c.321T>A	XP_011513732.1:p.Pro107=
NM_000535.6:c.639T>A	NP_000526.2:p.Pro213=
NM_001322003.1:c.234T>A	NP_001308932.1:p.Pro78=
NM_001322004.1:c.234T>A	NP_001308933.1:p.Pro78=
NM_001322005.1:c.234T>A	NP_001308934.1:p.Pro78=
NM_001322006.1:c.639T>A	NP_001308935.1:p.Pro213=
NM_001322007.1:c.321T>A	NP_001308936.1:p.Pro107=
NM_001322008.1:c.321T>A	NP_001308937.1:p.Pro107=
NM_001322009.1:c.234T>A	NP_001308938.1:p.Pro78=
NM_001322010.1:c.234T>A	NP_001308939.1:p.Pro78=
NM_001322011.1:c.-295T>A	NP_001308940.1:n.-295T>A
NM_001322012.1:c.-295T>A	NP_001308941.1:n.-295T>A
NM_001322013.1:c.133-1751T>A	NP_001308942.1:n.133-1751T>A
NM_001322014.1:c.639T>A	NP_001308943.1:p.Pro213=
NM_001322015.1:c.330T>A	NP_001308944.1:p.Pro110=
NR_136154.1:n.726T>A
XM_017012342.2:c.-195T>A	XP_016867831.1:n.-195T>A
XM_024446800.1:c.234T>A	XP_024302568.1:p.Pro78=
NM_000535.7:c.639T>A MANE Select	NP_000526.2:p.Pro213=
NM_001322003.2:c.234T>A	NP_001308932.1:p.Pro78=
NM_001322004.2:c.234T>A	NP_001308933.1:p.Pro78=
NM_001322005.2:c.234T>A	NP_001308934.1:p.Pro78=
NM_001322006.2:c.639T>A	NP_001308935.1:p.Pro213=
NM_001322008.2:c.321T>A	NP_001308937.1:p.Pro107=
NM_001322009.2:c.234T>A	NP_001308938.1:p.Pro78=
NM_001322010.2:c.234T>A	NP_001308939.1:p.Pro78=
NM_001322011.2:c.-295T>A	NP_001308940.1:n.-295T>A
NM_001322012.2:c.-295T>A	NP_001308941.1:n.-295T>A
NM_001322013.2:c.133-1751T>A	NP_001308942.1:n.133-1751T>A
NM_001322014.2:c.639T>A	NP_001308943.1:p.Pro213=
NM_001322015.2:c.330T>A	NP_001308944.1:p.Pro110=
NM_001322007.2:c.321T>A	NP_001308936.1:p.Pro107=