Canonical Allele Identifier: CA366738187

Gene: PMS2

Linked Data

• gnomAD v4: 7-5982984-T-C
• MyVariant Identifiers: chr7:g.6022615T>C (hg19) ; chr7:g.5982984T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5982984T>C , CM000669.2:g.5982984T>C	GRCh38
NC_000007.13:g.6022615T>C , CM000669.1:g.6022615T>C	GRCh37
NC_000007.12:g.5989141T>C	NCBI36
NG_008466.1:g.31123A>G , LRG_161:g.31123A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699814.2:c.*1410A>G	ENSP00000514615.2:n.*1410A>G
ENST00000699840.2:c.2011A>G	ENSP00000514638.2:p.Met671Val
ENST00000699930.2:c.1906A>G	ENSP00000514695.2:p.Met636Val
ENST00000406569.8:c.1678+4103A>G	ENSP00000514464.1:n.1678+4103A>G
ENST00000644110.2:c.*1608A>G	ENSP00000496392.2:n.*1608A>G
ENST00000699752.1:c.1858A>G	ENSP00000514561.1:p.Met620Val
ENST00000699753.1:c.*1435A>G	ENSP00000514562.1:n.*1435A>G
ENST00000699754.1:c.1816A>G	ENSP00000514563.1:p.Met606Val
ENST00000699755.1:c.*1413A>G	ENSP00000514564.1:n.*1413A>G
ENST00000699756.1:c.*1601A>G	ENSP00000514565.1:n.*1601A>G
ENST00000699757.1:c.*1271A>G	ENSP00000514566.1:n.*1271A>G
ENST00000699758.1:c.*1271A>G	ENSP00000514567.1:n.*1271A>G
ENST00000699759.1:n.2868A>G
ENST00000699760.1:c.1696A>G	ENSP00000514568.1:p.Met566Val
ENST00000699761.1:c.1609A>G	ENSP00000514569.1:p.Met537Val
ENST00000699762.1:c.1441A>G	ENSP00000514570.1:p.Met481Val
ENST00000699763.1:c.*1104A>G	ENSP00000514571.1:n.*1104A>G
ENST00000699764.1:c.*332A>G	ENSP00000514572.1:n.*332A>G
ENST00000699765.1:c.*1110A>G	ENSP00000514573.1:n.*1110A>G
ENST00000699766.1:c.2014A>G	ENSP00000514574.1:p.Met672Val
ENST00000699767.1:c.2014A>G	ENSP00000514575.1:p.Met672Val
ENST00000699768.1:c.2014A>G	ENSP00000514576.1:p.Met672Val
ENST00000699811.1:c.1609A>G	ENSP00000514614.1:p.Met537Val
ENST00000699813.1:n.2127A>G
ENST00000699814.1:c.1637A>G
ENST00000699815.1:c.*1545A>G	ENSP00000514616.1:n.*1545A>G
ENST00000699816.1:c.*904A>G	ENSP00000514617.1:n.*904A>G
ENST00000699817.1:c.*1608A>G	ENSP00000514618.1:n.*1608A>G
ENST00000699818.1:c.1609A>G	ENSP00000514619.1:p.Met537Val
ENST00000699819.1:c.*1171A>G	ENSP00000514620.1:n.*1171A>G
ENST00000699820.1:c.1152A>G	ENSP00000514621.1:p.Arg384=
ENST00000699821.1:c.1609A>G	ENSP00000514622.1:p.Met537Val
ENST00000699822.1:c.*1466A>G	ENSP00000514623.1:n.*1466A>G
ENST00000699823.1:c.1609A>G	ENSP00000514624.1:p.Met537Val
ENST00000699824.1:c.*1517A>G	ENSP00000514625.1:n.*1517A>G
ENST00000699825.1:c.1453A>G	ENSP00000514626.1:p.Met485Val
ENST00000699826.1:c.*1413A>G	ENSP00000514627.1:n.*1413A>G
ENST00000699827.1:c.1846A>G	ENSP00000514628.1:p.Met616Val
ENST00000699828.1:c.*1104A>G	ENSP00000514629.1:n.*1104A>G
ENST00000699833.1:n.3786A>G
ENST00000699837.1:c.1609A>G	ENSP00000514635.1:p.Met537Val
ENST00000699838.1:c.*1914A>G	ENSP00000514636.1:n.*1914A>G
ENST00000699839.1:c.2200A>G	ENSP00000514637.1:p.Met734Val
ENST00000699916.1:c.*1271A>G	ENSP00000514684.1:n.*1271A>G
ENST00000699917.1:c.*1463A>G	ENSP00000514685.1:n.*1463A>G
ENST00000699918.1:c.*1515A>G	ENSP00000514686.1:n.*1515A>G
ENST00000699919.1:c.*1601A>G	ENSP00000514687.1:n.*1601A>G
ENST00000699920.1:c.*1650A>G	ENSP00000514688.1:n.*1650A>G
ENST00000699928.1:c.996A>G	ENSP00000514693.1:p.Arg332=
ENST00000699951.1:c.*1110A>G	ENSP00000514706.1:n.*1110A>G
ENST00000699952.1:c.804-9442A>G	ENSP00000514707.1:n.804-9442A>G
ENST00000265849.12:c.2014A>G MANE Select	ENSP00000265849.7:p.Met672Val
ENST00000642292.1:c.1609A>G	ENSP00000495524.1:p.Met537Val
ENST00000642456.1:c.1609A>G	ENSP00000493814.1:p.Met537Val
ENST00000643595.1:c.*1413A>G	ENSP00000494497.1:n.*1413A>G
ENST00000644110.1:c.1696A>G	ENSP00000496392.1:p.Met566Val
ENST00000265849.11:c.2014A>G	ENSP00000265849.7:p.Met672Val
ENST00000382321.5:c.811A>G	ENSP00000371758.4:p.Met271Val
ENST00000406569.7:n.1678+4103A>G
ENST00000441476.6:c.1696A>G	ENSP00000392843.2:p.Met566Val
ENST00000469652.1:n.63-79A>G
NM_000535.5:c.2014A>G , LRG_161t1:c.2014A>G	NP_000526.1:p.Met672Val
NR_003085.2:n.2096A>G
XM_006715742.2:c.2008A>G	XP_006715805.1:p.Met670Val
XM_006715744.2:c.1081A>G	XP_006715807.1:p.Met361Val
XM_011515427.1:c.2059A>G	XP_011513729.1:p.Met687Val
XM_011515428.1:c.1903A>G	XP_011513730.1:p.Met635Val
XM_011515429.1:c.1696A>G	XP_011513731.1:p.Met566Val
XM_011515430.1:c.1696A>G	XP_011513732.1:p.Met566Val
NM_000535.6:c.2014A>G	NP_000526.2:p.Met672Val
NM_001322003.1:c.1609A>G	NP_001308932.1:p.Met537Val
NM_001322004.1:c.1609A>G	NP_001308933.1:p.Met537Val
NM_001322005.1:c.1609A>G	NP_001308934.1:p.Met537Val
NM_001322006.1:c.1858A>G	NP_001308935.1:p.Met620Val
NM_001322007.1:c.1696A>G	NP_001308936.1:p.Met566Val
NM_001322008.1:c.1696A>G	NP_001308937.1:p.Met566Val
NM_001322009.1:c.1609A>G	NP_001308938.1:p.Met537Val
NM_001322010.1:c.1453A>G	NP_001308939.1:p.Met485Val
NM_001322011.1:c.1081A>G	NP_001308940.1:p.Met361Val
NM_001322012.1:c.1081A>G	NP_001308941.1:p.Met361Val
NM_001322013.1:c.1441A>G	NP_001308942.1:p.Met481Val
NM_001322014.1:c.2014A>G	NP_001308943.1:p.Met672Val
NM_001322015.1:c.1705A>G	NP_001308944.1:p.Met569Val
NR_136154.1:n.2101A>G
XM_006715744.4:c.1081A>G	XP_006715807.1:p.Met361Val
XM_017012342.2:c.1081A>G	XP_016867831.1:p.Met361Val
XM_024446800.1:c.1453A>G	XP_024302568.1:p.Met485Val
NM_000535.7:c.2014A>G MANE Select	NP_000526.2:p.Met672Val
NM_001322003.2:c.1609A>G	NP_001308932.1:p.Met537Val
NM_001322004.2:c.1609A>G	NP_001308933.1:p.Met537Val
NM_001322005.2:c.1609A>G	NP_001308934.1:p.Met537Val
NM_001322006.2:c.1858A>G	NP_001308935.1:p.Met620Val
NM_001322008.2:c.1696A>G	NP_001308937.1:p.Met566Val
NM_001322009.2:c.1609A>G	NP_001308938.1:p.Met537Val
NM_001322010.2:c.1453A>G	NP_001308939.1:p.Met485Val
NM_001322011.2:c.1081A>G	NP_001308940.1:p.Met361Val
NM_001322012.2:c.1081A>G	NP_001308941.1:p.Met361Val
NM_001322013.2:c.1441A>G	NP_001308942.1:p.Met481Val
NM_001322014.2:c.2014A>G	NP_001308943.1:p.Met672Val
NM_001322015.2:c.1705A>G	NP_001308944.1:p.Met569Val
NM_001322007.2:c.1696A>G	NP_001308936.1:p.Met566Val