Canonical Allele Identifier: CA1685250496
Gene: PMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5977695G= , CM000669.2:g.5977695G= GRCh38
NC_000007.13:g.6017326G= , CM000669.1:g.6017326G= GRCh37
NC_000007.12:g.5983852G= NCBI36
NG_008466.1:g.36412C= , LRG_161:g.36412C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*1734C= ENSP00000514615.2:n.*1734C=
ENST00000699840.2:c.2335C= ENSP00000514638.2:p.Pro779=
ENST00000699930.2:c.2230C= ENSP00000514695.2:p.Pro744=
ENST00000406569.8:c.1698C= ENSP00000514464.1:p.Asp566=
ENST00000644110.2:c.*1932C= ENSP00000496392.2:n.*1932C=
ENST00000699752.1:c.2182C= ENSP00000514561.1:p.Pro728=
ENST00000699753.1:c.*1759C= ENSP00000514562.1:n.*1759C=
ENST00000699754.1:c.2140C= ENSP00000514563.1:p.Pro714=
ENST00000699755.1:c.*1737C= ENSP00000514564.1:n.*1737C=
ENST00000699756.1:c.*1925C= ENSP00000514565.1:n.*1925C=
ENST00000699757.1:c.*1595C= ENSP00000514566.1:n.*1595C=
ENST00000699758.1:c.*1595C= ENSP00000514567.1:n.*1595C=
ENST00000699759.1:n.3192C=
ENST00000699760.1:c.2020C= ENSP00000514568.1:p.Pro674=
ENST00000699761.1:c.1933C= ENSP00000514569.1:p.Pro645=
ENST00000699762.1:c.1765C= ENSP00000514570.1:p.Pro589=
ENST00000699763.1:c.*1428C= ENSP00000514571.1:n.*1428C=
ENST00000699764.1:c.*656C= ENSP00000514572.1:n.*656C=
ENST00000699765.1:c.*1333C= ENSP00000514573.1:n.*1333C=
ENST00000699766.1:c.2371C= ENSP00000514574.1:p.Pro791=
ENST00000699767.1:c.2295C= ENSP00000514575.1:p.Asp765=
ENST00000699768.1:c.2194C= ENSP00000514576.1:p.Pro732=
ENST00000699811.1:c.1933C= ENSP00000514614.1:p.Pro645=
ENST00000699813.1:n.2451C=
ENST00000699814.1:c.1961C=
ENST00000699815.1:c.*1869C= ENSP00000514616.1:n.*1869C=
ENST00000699816.1:c.*1228C= ENSP00000514617.1:n.*1228C=
ENST00000699817.1:c.*1932C= ENSP00000514618.1:n.*1932C=
ENST00000699818.1:c.1933C= ENSP00000514619.1:p.Pro645=
ENST00000699819.1:c.*1495C= ENSP00000514620.1:n.*1495C=
ENST00000699820.1:c.*276C= ENSP00000514621.1:n.*276C=
ENST00000699821.1:c.1966C= ENSP00000514622.1:p.Pro656=
ENST00000699822.1:c.*1790C= ENSP00000514623.1:n.*1790C=
ENST00000699823.1:c.1933C= ENSP00000514624.1:p.Pro645=
ENST00000699824.1:c.*1841C= ENSP00000514625.1:n.*1841C=
ENST00000699825.1:c.1777C= ENSP00000514626.1:p.Pro593=
ENST00000699826.1:c.*1737C= ENSP00000514627.1:n.*1737C=
ENST00000699827.1:c.2170C= ENSP00000514628.1:p.Pro724=
ENST00000699828.1:c.*1428C= ENSP00000514629.1:n.*1428C=
ENST00000699833.1:n.4110C=
ENST00000699837.1:c.1933C= ENSP00000514635.1:p.Pro645=
ENST00000699838.1:c.*2238C= ENSP00000514636.1:n.*2238C=
ENST00000699839.1:c.2524C= ENSP00000514637.1:p.Pro842=
ENST00000699916.1:c.*1595C= ENSP00000514684.1:n.*1595C=
ENST00000699917.1:c.*1787C= ENSP00000514685.1:n.*1787C=
ENST00000699918.1:c.*1839C= ENSP00000514686.1:n.*1839C=
ENST00000699919.1:c.*1925C= ENSP00000514687.1:n.*1925C=
ENST00000699920.1:c.*1974C= ENSP00000514688.1:n.*1974C=
ENST00000699928.1:c.*276C= ENSP00000514693.1:n.*276C=
ENST00000699951.1:c.*1391C= ENSP00000514706.1:n.*1391C=
ENST00000699952.1:c.804-4153C= ENSP00000514707.1:n.804-4153C=
ENST00000265849.12:c.2338C= MANE Select ENSP00000265849.7:p.Pro780=
ENST00000642292.1:c.1933C= ENSP00000495524.1:p.Pro645=
ENST00000642456.1:c.1933C= ENSP00000493814.1:p.Pro645=
ENST00000643595.1:c.*1737C= ENSP00000494497.1:n.*1737C=
ENST00000644110.1:c.2020C= ENSP00000496392.1:p.Pro674=
ENST00000265849.11:c.2338C= ENSP00000265849.7:p.Pro780=
ENST00000382321.5:c.1135C= ENSP00000371758.4:p.Pro379=
ENST00000406569.7:n.1698C=
ENST00000441476.6:c.2020C= ENSP00000392843.2:p.Pro674=
NM_000535.5:c.2338C= , LRG_161t1:c.2338C= NP_000526.1:p.Pro780=
NR_003085.2:n.2420C=
XM_006715742.2:c.2332C= XP_006715805.1:p.Pro778=
XM_006715744.2:c.1405C= XP_006715807.1:p.Pro469=
XM_011515427.1:c.2383C= XP_011513729.1:p.Pro795=
XM_011515428.1:c.2227C= XP_011513730.1:p.Pro743=
XM_011515429.1:c.2020C= XP_011513731.1:p.Pro674=
XM_011515430.1:c.2020C= XP_011513732.1:p.Pro674=
NM_000535.6:c.2338C= NP_000526.2:p.Pro780=
NM_001322003.1:c.1933C= NP_001308932.1:p.Pro645=
NM_001322004.1:c.1933C= NP_001308933.1:p.Pro645=
NM_001322005.1:c.1933C= NP_001308934.1:p.Pro645=
NM_001322006.1:c.2182C= NP_001308935.1:p.Pro728=
NM_001322007.1:c.2020C= NP_001308936.1:p.Pro674=
NM_001322008.1:c.2020C= NP_001308937.1:p.Pro674=
NM_001322009.1:c.1966C= NP_001308938.1:p.Pro656=
NM_001322010.1:c.1777C= NP_001308939.1:p.Pro593=
NM_001322011.1:c.1405C= NP_001308940.1:p.Pro469=
NM_001322012.1:c.1405C= NP_001308941.1:p.Pro469=
NM_001322013.1:c.1765C= NP_001308942.1:p.Pro589=
NM_001322014.1:c.2371C= NP_001308943.1:p.Pro791=
NM_001322015.1:c.2029C= NP_001308944.1:p.Pro677=
NR_136154.1:n.2382C=
XM_006715744.4:c.1405C= XP_006715807.1:p.Pro469=
XM_017012342.2:c.1405C= XP_016867831.1:p.Pro469=
XM_024446800.1:c.1777C= XP_024302568.1:p.Pro593=
NM_000535.7:c.2338C= MANE Select NP_000526.2:p.Pro780=
NM_001322003.2:c.1933C= NP_001308932.1:p.Pro645=
NM_001322004.2:c.1933C= NP_001308933.1:p.Pro645=
NM_001322005.2:c.1933C= NP_001308934.1:p.Pro645=
NM_001322006.2:c.2182C= NP_001308935.1:p.Pro728=
NM_001322008.2:c.2020C= NP_001308937.1:p.Pro674=
NM_001322009.2:c.1966C= NP_001308938.1:p.Pro656=
NM_001322010.2:c.1777C= NP_001308939.1:p.Pro593=
NM_001322011.2:c.1405C= NP_001308940.1:p.Pro469=
NM_001322012.2:c.1405C= NP_001308941.1:p.Pro469=
NM_001322013.2:c.1765C= NP_001308942.1:p.Pro589=
NM_001322014.2:c.2371C= NP_001308943.1:p.Pro791=
NM_001322015.2:c.2029C= NP_001308944.1:p.Pro677=
NM_001322007.2:c.2020C= NP_001308936.1:p.Pro674=