Canonical Allele Identifier: CA1685217928
Gene: PMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5982985C= , CM000669.2:g.5982985C= GRCh38
NC_000007.13:g.6022616C= , CM000669.1:g.6022616C= GRCh37
NC_000007.12:g.5989142C= NCBI36
NG_008466.1:g.31122G= , LRG_161:g.31122G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*1409G= ENSP00000514615.2:n.*1409G=
ENST00000699840.2:c.2010G= ENSP00000514638.2:p.Thr670=
ENST00000699930.2:c.1905G= ENSP00000514695.2:p.Thr635=
ENST00000406569.8:c.1678+4102G= ENSP00000514464.1:n.1678+4102G=
ENST00000644110.2:c.*1607G= ENSP00000496392.2:n.*1607G=
ENST00000699752.1:c.1857G= ENSP00000514561.1:p.Thr619=
ENST00000699753.1:c.*1434G= ENSP00000514562.1:n.*1434G=
ENST00000699754.1:c.1815G= ENSP00000514563.1:p.Thr605=
ENST00000699755.1:c.*1412G= ENSP00000514564.1:n.*1412G=
ENST00000699756.1:c.*1600G= ENSP00000514565.1:n.*1600G=
ENST00000699757.1:c.*1270G= ENSP00000514566.1:n.*1270G=
ENST00000699758.1:c.*1270G= ENSP00000514567.1:n.*1270G=
ENST00000699759.1:n.2867G=
ENST00000699760.1:c.1695G= ENSP00000514568.1:p.Thr565=
ENST00000699761.1:c.1608G= ENSP00000514569.1:p.Thr536=
ENST00000699762.1:c.1440G= ENSP00000514570.1:p.Thr480=
ENST00000699763.1:c.*1103G= ENSP00000514571.1:n.*1103G=
ENST00000699764.1:c.*331G= ENSP00000514572.1:n.*331G=
ENST00000699765.1:c.*1109G= ENSP00000514573.1:n.*1109G=
ENST00000699766.1:c.2013G= ENSP00000514574.1:p.Thr671=
ENST00000699767.1:c.2013G= ENSP00000514575.1:p.Thr671=
ENST00000699768.1:c.2013G= ENSP00000514576.1:p.Thr671=
ENST00000699811.1:c.1608G= ENSP00000514614.1:p.Thr536=
ENST00000699813.1:n.2126G=
ENST00000699814.1:c.1636G=
ENST00000699815.1:c.*1544G= ENSP00000514616.1:n.*1544G=
ENST00000699816.1:c.*903G= ENSP00000514617.1:n.*903G=
ENST00000699817.1:c.*1607G= ENSP00000514618.1:n.*1607G=
ENST00000699818.1:c.1608G= ENSP00000514619.1:p.Thr536=
ENST00000699819.1:c.*1170G= ENSP00000514620.1:n.*1170G=
ENST00000699820.1:c.1151G= ENSP00000514621.1:p.Arg384=
ENST00000699821.1:c.1608G= ENSP00000514622.1:p.Thr536=
ENST00000699822.1:c.*1465G= ENSP00000514623.1:n.*1465G=
ENST00000699823.1:c.1608G= ENSP00000514624.1:p.Thr536=
ENST00000699824.1:c.*1516G= ENSP00000514625.1:n.*1516G=
ENST00000699825.1:c.1452G= ENSP00000514626.1:p.Thr484=
ENST00000699826.1:c.*1412G= ENSP00000514627.1:n.*1412G=
ENST00000699827.1:c.1845G= ENSP00000514628.1:p.Thr615=
ENST00000699828.1:c.*1103G= ENSP00000514629.1:n.*1103G=
ENST00000699833.1:n.3785G=
ENST00000699837.1:c.1608G= ENSP00000514635.1:p.Thr536=
ENST00000699838.1:c.*1913G= ENSP00000514636.1:n.*1913G=
ENST00000699839.1:c.2199G= ENSP00000514637.1:p.Thr733=
ENST00000699916.1:c.*1270G= ENSP00000514684.1:n.*1270G=
ENST00000699917.1:c.*1462G= ENSP00000514685.1:n.*1462G=
ENST00000699918.1:c.*1514G= ENSP00000514686.1:n.*1514G=
ENST00000699919.1:c.*1600G= ENSP00000514687.1:n.*1600G=
ENST00000699920.1:c.*1649G= ENSP00000514688.1:n.*1649G=
ENST00000699928.1:c.995G= ENSP00000514693.1:p.Arg332=
ENST00000699951.1:c.*1109G= ENSP00000514706.1:n.*1109G=
ENST00000699952.1:c.804-9443G= ENSP00000514707.1:n.804-9443G=
ENST00000265849.12:c.2013G= MANE Select ENSP00000265849.7:p.Thr671=
ENST00000642292.1:c.1608G= ENSP00000495524.1:p.Thr536=
ENST00000642456.1:c.1608G= ENSP00000493814.1:p.Thr536=
ENST00000643595.1:c.*1412G= ENSP00000494497.1:n.*1412G=
ENST00000644110.1:c.1695G= ENSP00000496392.1:p.Thr565=
ENST00000265849.11:c.2013G= ENSP00000265849.7:p.Thr671=
ENST00000382321.5:c.810G= ENSP00000371758.4:p.Thr270=
ENST00000406569.7:n.1678+4102G=
ENST00000441476.6:c.1695G= ENSP00000392843.2:p.Thr565=
ENST00000469652.1:n.63-80G=
NM_000535.5:c.2013G= , LRG_161t1:c.2013G= NP_000526.1:p.Thr671=
NR_003085.2:n.2095G=
XM_006715742.2:c.2007G= XP_006715805.1:p.Thr669=
XM_006715744.2:c.1080G= XP_006715807.1:p.Thr360=
XM_011515427.1:c.2058G= XP_011513729.1:p.Thr686=
XM_011515428.1:c.1902G= XP_011513730.1:p.Thr634=
XM_011515429.1:c.1695G= XP_011513731.1:p.Thr565=
XM_011515430.1:c.1695G= XP_011513732.1:p.Thr565=
NM_000535.6:c.2013G= NP_000526.2:p.Thr671=
NM_001322003.1:c.1608G= NP_001308932.1:p.Thr536=
NM_001322004.1:c.1608G= NP_001308933.1:p.Thr536=
NM_001322005.1:c.1608G= NP_001308934.1:p.Thr536=
NM_001322006.1:c.1857G= NP_001308935.1:p.Thr619=
NM_001322007.1:c.1695G= NP_001308936.1:p.Thr565=
NM_001322008.1:c.1695G= NP_001308937.1:p.Thr565=
NM_001322009.1:c.1608G= NP_001308938.1:p.Thr536=
NM_001322010.1:c.1452G= NP_001308939.1:p.Thr484=
NM_001322011.1:c.1080G= NP_001308940.1:p.Thr360=
NM_001322012.1:c.1080G= NP_001308941.1:p.Thr360=
NM_001322013.1:c.1440G= NP_001308942.1:p.Thr480=
NM_001322014.1:c.2013G= NP_001308943.1:p.Thr671=
NM_001322015.1:c.1704G= NP_001308944.1:p.Thr568=
NR_136154.1:n.2100G=
XM_006715744.4:c.1080G= XP_006715807.1:p.Thr360=
XM_017012342.2:c.1080G= XP_016867831.1:p.Thr360=
XM_024446800.1:c.1452G= XP_024302568.1:p.Thr484=
NM_000535.7:c.2013G= MANE Select NP_000526.2:p.Thr671=
NM_001322003.2:c.1608G= NP_001308932.1:p.Thr536=
NM_001322004.2:c.1608G= NP_001308933.1:p.Thr536=
NM_001322005.2:c.1608G= NP_001308934.1:p.Thr536=
NM_001322006.2:c.1857G= NP_001308935.1:p.Thr619=
NM_001322008.2:c.1695G= NP_001308937.1:p.Thr565=
NM_001322009.2:c.1608G= NP_001308938.1:p.Thr536=
NM_001322010.2:c.1452G= NP_001308939.1:p.Thr484=
NM_001322011.2:c.1080G= NP_001308940.1:p.Thr360=
NM_001322012.2:c.1080G= NP_001308941.1:p.Thr360=
NM_001322013.2:c.1440G= NP_001308942.1:p.Thr480=
NM_001322014.2:c.2013G= NP_001308943.1:p.Thr671=
NM_001322015.2:c.1704G= NP_001308944.1:p.Thr568=
NM_001322007.2:c.1695G= NP_001308936.1:p.Thr565=