Canonical Allele Identifier: CA366738013
Gene: PMS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496035
ClinVar RCV Id: RCV000586329
dbSNP Id: rs751551006

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5982906C>T , CM000669.2:g.5982906C>T GRCh38
NC_000007.13:g.6022537C>T , CM000669.1:g.6022537C>T GRCh37
NC_000007.12:g.5989063C>T NCBI36
NG_008466.1:g.31201G>A , LRG_161:g.31201G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000699814.2:c.*1488G>A ENSP00000514615.2:n.*1488G>A
ENST00000699840.2:c.2089G>A ENSP00000514638.2:p.Val697Met
ENST00000699930.2:c.1984G>A ENSP00000514695.2:p.Val662Met
ENST00000406569.8:c.1678+4181G>A ENSP00000514464.1:n.1678+4181G>A
ENST00000644110.2:c.*1686G>A ENSP00000496392.2:n.*1686G>A
ENST00000699752.1:c.1936G>A ENSP00000514561.1:p.Val646Met
ENST00000699753.1:c.*1513G>A ENSP00000514562.1:n.*1513G>A
ENST00000699754.1:c.1894G>A ENSP00000514563.1:p.Val632Met
ENST00000699755.1:c.*1491G>A ENSP00000514564.1:n.*1491G>A
ENST00000699756.1:c.*1679G>A ENSP00000514565.1:n.*1679G>A
ENST00000699757.1:c.*1349G>A ENSP00000514566.1:n.*1349G>A
ENST00000699758.1:c.*1349G>A ENSP00000514567.1:n.*1349G>A
ENST00000699759.1:n.2946G>A
ENST00000699760.1:c.1774G>A ENSP00000514568.1:p.Val592Met
ENST00000699761.1:c.1687G>A ENSP00000514569.1:p.Val563Met
ENST00000699762.1:c.1519G>A ENSP00000514570.1:p.Val507Met
ENST00000699763.1:c.*1182G>A ENSP00000514571.1:n.*1182G>A
ENST00000699764.1:c.*410G>A ENSP00000514572.1:n.*410G>A
ENST00000699765.1:c.*1188G>A ENSP00000514573.1:n.*1188G>A
ENST00000699766.1:c.2092G>A ENSP00000514574.1:p.Val698Met
ENST00000699767.1:c.2092G>A ENSP00000514575.1:p.Val698Met
ENST00000699768.1:c.2092G>A ENSP00000514576.1:p.Val698Met
ENST00000699811.1:c.1687G>A ENSP00000514614.1:p.Val563Met
ENST00000699813.1:n.2205G>A
ENST00000699814.1:c.1715G>A
ENST00000699815.1:c.*1623G>A ENSP00000514616.1:n.*1623G>A
ENST00000699816.1:c.*982G>A ENSP00000514617.1:n.*982G>A
ENST00000699817.1:c.*1686G>A ENSP00000514618.1:n.*1686G>A
ENST00000699818.1:c.1687G>A ENSP00000514619.1:p.Val563Met
ENST00000699819.1:c.*1249G>A ENSP00000514620.1:n.*1249G>A
ENST00000699820.1:c.*30G>A ENSP00000514621.1:n.*30G>A
ENST00000699821.1:c.1687G>A ENSP00000514622.1:p.Val563Met
ENST00000699822.1:c.*1544G>A ENSP00000514623.1:n.*1544G>A
ENST00000699823.1:c.1687G>A ENSP00000514624.1:p.Val563Met
ENST00000699824.1:c.*1595G>A ENSP00000514625.1:n.*1595G>A
ENST00000699825.1:c.1531G>A ENSP00000514626.1:p.Val511Met
ENST00000699826.1:c.*1491G>A ENSP00000514627.1:n.*1491G>A
ENST00000699827.1:c.1924G>A ENSP00000514628.1:p.Val642Met
ENST00000699828.1:c.*1182G>A ENSP00000514629.1:n.*1182G>A
ENST00000699833.1:n.3864G>A
ENST00000699837.1:c.1687G>A ENSP00000514635.1:p.Val563Met
ENST00000699838.1:c.*1992G>A ENSP00000514636.1:n.*1992G>A
ENST00000699839.1:c.2278G>A ENSP00000514637.1:p.Val760Met
ENST00000699916.1:c.*1349G>A ENSP00000514684.1:n.*1349G>A
ENST00000699917.1:c.*1541G>A ENSP00000514685.1:n.*1541G>A
ENST00000699918.1:c.*1593G>A ENSP00000514686.1:n.*1593G>A
ENST00000699919.1:c.*1679G>A ENSP00000514687.1:n.*1679G>A
ENST00000699920.1:c.*1728G>A ENSP00000514688.1:n.*1728G>A
ENST00000699928.1:c.*30G>A ENSP00000514693.1:n.*30G>A
ENST00000699951.1:c.*1188G>A ENSP00000514706.1:n.*1188G>A
ENST00000699952.1:c.804-9364G>A ENSP00000514707.1:n.804-9364G>A
ENST00000265849.12:c.2092G>A MANE Select ENSP00000265849.7:p.Val698Met
ENST00000642292.1:c.1687G>A ENSP00000495524.1:p.Val563Met
ENST00000642456.1:c.1687G>A ENSP00000493814.1:p.Val563Met
ENST00000643595.1:c.*1491G>A ENSP00000494497.1:n.*1491G>A
ENST00000644110.1:c.1774G>A ENSP00000496392.1:p.Val592Met
ENST00000265849.11:c.2092G>A ENSP00000265849.7:p.Val698Met
ENST00000382321.5:c.889G>A ENSP00000371758.4:p.Val297Met
ENST00000406569.7:n.1678+4181G>A
ENST00000441476.6:c.1774G>A ENSP00000392843.2:p.Val592Met
ENST00000469652.1:n.63-1G>A
NM_000535.5:c.2092G>A , LRG_161t1:c.2092G>A NP_000526.1:p.Val698Met
NR_003085.2:n.2174G>A
XM_006715742.2:c.2086G>A XP_006715805.1:p.Val696Met
XM_006715744.2:c.1159G>A XP_006715807.1:p.Val387Met
XM_011515427.1:c.2137G>A XP_011513729.1:p.Val713Met
XM_011515428.1:c.1981G>A XP_011513730.1:p.Val661Met
XM_011515429.1:c.1774G>A XP_011513731.1:p.Val592Met
XM_011515430.1:c.1774G>A XP_011513732.1:p.Val592Met
NM_000535.6:c.2092G>A NP_000526.2:p.Val698Met
NM_001322003.1:c.1687G>A NP_001308932.1:p.Val563Met
NM_001322004.1:c.1687G>A NP_001308933.1:p.Val563Met
NM_001322005.1:c.1687G>A NP_001308934.1:p.Val563Met
NM_001322006.1:c.1936G>A NP_001308935.1:p.Val646Met
NM_001322007.1:c.1774G>A NP_001308936.1:p.Val592Met
NM_001322008.1:c.1774G>A NP_001308937.1:p.Val592Met
NM_001322009.1:c.1687G>A NP_001308938.1:p.Val563Met
NM_001322010.1:c.1531G>A NP_001308939.1:p.Val511Met
NM_001322011.1:c.1159G>A NP_001308940.1:p.Val387Met
NM_001322012.1:c.1159G>A NP_001308941.1:p.Val387Met
NM_001322013.1:c.1519G>A NP_001308942.1:p.Val507Met
NM_001322014.1:c.2092G>A NP_001308943.1:p.Val698Met
NM_001322015.1:c.1783G>A NP_001308944.1:p.Val595Met
NR_136154.1:n.2179G>A
XM_006715744.4:c.1159G>A XP_006715807.1:p.Val387Met
XM_017012342.2:c.1159G>A XP_016867831.1:p.Val387Met
XM_024446800.1:c.1531G>A XP_024302568.1:p.Val511Met
NM_000535.7:c.2092G>A MANE Select NP_000526.2:p.Val698Met
NM_001322003.2:c.1687G>A NP_001308932.1:p.Val563Met
NM_001322004.2:c.1687G>A NP_001308933.1:p.Val563Met
NM_001322005.2:c.1687G>A NP_001308934.1:p.Val563Met
NM_001322006.2:c.1936G>A NP_001308935.1:p.Val646Met
NM_001322008.2:c.1774G>A NP_001308937.1:p.Val592Met
NM_001322009.2:c.1687G>A NP_001308938.1:p.Val563Met
NM_001322010.2:c.1531G>A NP_001308939.1:p.Val511Met
NM_001322011.2:c.1159G>A NP_001308940.1:p.Val387Met
NM_001322012.2:c.1159G>A NP_001308941.1:p.Val387Met
NM_001322013.2:c.1519G>A NP_001308942.1:p.Val507Met
NM_001322014.2:c.2092G>A NP_001308943.1:p.Val698Met
NM_001322015.2:c.1783G>A NP_001308944.1:p.Val595Met
NM_001322007.2:c.1774G>A NP_001308936.1:p.Val592Met