Canonical Allele Identifier: CA366742084
Gene: PMS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046169
dbSNP Id: rs1783101060

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5987356G>A , CM000669.2:g.5987356G>A GRCh38
NC_000007.13:g.6026987G>A , CM000669.1:g.6026987G>A GRCh37
NC_000007.12:g.5993513G>A NCBI36
NG_008466.1:g.26751C>T , LRG_161:g.26751C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*805C>T ENSP00000514615.2:n.*805C>T
ENST00000699840.2:c.1406C>T ENSP00000514638.2:p.Pro469Leu
ENST00000699930.2:c.1301C>T ENSP00000514695.2:p.Pro434Leu
ENST00000406569.8:c.1409C>T ENSP00000514464.1:p.Pro470Leu
ENST00000644110.2:c.*1003C>T ENSP00000496392.2:n.*1003C>T
ENST00000699752.1:c.1253C>T ENSP00000514561.1:p.Pro418Leu
ENST00000699753.1:c.*830C>T ENSP00000514562.1:n.*830C>T
ENST00000699754.1:c.1211C>T ENSP00000514563.1:p.Pro404Leu
ENST00000699755.1:c.*808C>T ENSP00000514564.1:n.*808C>T
ENST00000699756.1:c.*996C>T ENSP00000514565.1:n.*996C>T
ENST00000699757.1:c.*666C>T ENSP00000514566.1:n.*666C>T
ENST00000699758.1:c.*666C>T ENSP00000514567.1:n.*666C>T
ENST00000699759.1:n.2263C>T
ENST00000699760.1:c.1091C>T ENSP00000514568.1:p.Pro364Leu
ENST00000699761.1:c.1004C>T ENSP00000514569.1:p.Pro335Leu
ENST00000699762.1:c.836C>T ENSP00000514570.1:p.Pro279Leu
ENST00000699763.1:c.*499C>T ENSP00000514571.1:n.*499C>T
ENST00000699764.1:c.1409C>T ENSP00000514572.1:p.Pro470Leu
ENST00000699765.1:c.*505C>T ENSP00000514573.1:n.*505C>T
ENST00000699766.1:c.1409C>T ENSP00000514574.1:p.Pro470Leu
ENST00000699767.1:c.1409C>T ENSP00000514575.1:p.Pro470Leu
ENST00000699768.1:c.1409C>T ENSP00000514576.1:p.Pro470Leu
ENST00000699811.1:c.1004C>T ENSP00000514614.1:p.Pro335Leu
ENST00000699813.1:n.1522C>T
ENST00000699814.1:c.1032C>T
ENST00000699815.1:c.*940C>T ENSP00000514616.1:n.*940C>T
ENST00000699816.1:c.*299C>T ENSP00000514617.1:n.*299C>T
ENST00000699817.1:c.*1003C>T ENSP00000514618.1:n.*1003C>T
ENST00000699818.1:c.1004C>T ENSP00000514619.1:p.Pro335Leu
ENST00000699819.1:c.*566C>T ENSP00000514620.1:n.*566C>T
ENST00000699820.1:c.1144+2444C>T ENSP00000514621.1:n.1144+2444C>T
ENST00000699821.1:c.1004C>T ENSP00000514622.1:p.Pro335Leu
ENST00000699822.1:c.*861C>T ENSP00000514623.1:n.*861C>T
ENST00000699823.1:c.1004C>T ENSP00000514624.1:p.Pro335Leu
ENST00000699824.1:c.*912C>T ENSP00000514625.1:n.*912C>T
ENST00000699825.1:c.848C>T ENSP00000514626.1:p.Pro283Leu
ENST00000699826.1:c.*808C>T ENSP00000514627.1:n.*808C>T
ENST00000699827.1:c.1241C>T ENSP00000514628.1:p.Pro414Leu
ENST00000699828.1:c.*499C>T ENSP00000514629.1:n.*499C>T
ENST00000699833.1:n.3181C>T
ENST00000699837.1:c.1004C>T ENSP00000514635.1:p.Pro335Leu
ENST00000699838.1:c.*1309C>T ENSP00000514636.1:n.*1309C>T
ENST00000699839.1:c.1595C>T ENSP00000514637.1:p.Pro532Leu
ENST00000699916.1:c.*666C>T ENSP00000514684.1:n.*666C>T
ENST00000699917.1:c.*858C>T ENSP00000514685.1:n.*858C>T
ENST00000699918.1:c.*910C>T ENSP00000514686.1:n.*910C>T
ENST00000699919.1:c.*996C>T ENSP00000514687.1:n.*996C>T
ENST00000699920.1:c.*1045C>T ENSP00000514688.1:n.*1045C>T
ENST00000699928.1:c.989-4365C>T ENSP00000514693.1:n.989-4365C>T
ENST00000699929.1:c.*710C>T ENSP00000514694.1:n.*710C>T
ENST00000699930.1:c.1301C>T ENSP00000514695.1:p.Pro434Leu
ENST00000699931.1:n.2837C>T
ENST00000699951.1:c.*505C>T ENSP00000514706.1:n.*505C>T
ENST00000699952.1:c.803+9970C>T ENSP00000514707.1:n.803+9970C>T
ENST00000699953.1:c.*516C>T ENSP00000514708.1:n.*516C>T
ENST00000699954.1:c.*710C>T ENSP00000514709.1:n.*710C>T
ENST00000265849.12:c.1409C>T MANE Select ENSP00000265849.7:p.Pro470Leu
ENST00000642292.1:c.1004C>T ENSP00000495524.1:p.Pro335Leu
ENST00000642456.1:c.1004C>T ENSP00000493814.1:p.Pro335Leu
ENST00000643595.1:c.*808C>T ENSP00000494497.1:n.*808C>T
ENST00000644110.1:c.1091C>T ENSP00000496392.1:p.Pro364Leu
ENST00000265849.11:c.1409C>T ENSP00000265849.7:p.Pro470Leu
ENST00000382321.5:c.804-4365C>T ENSP00000371758.4:n.804-4365C>T
ENST00000406569.7:n.1409C>T
ENST00000441476.6:c.1091C>T ENSP00000392843.2:p.Pro364Leu
ENST00000469652.1:n.63-4451C>T
NM_000535.5:c.1409C>T , LRG_161t1:c.1409C>T NP_000526.1:p.Pro470Leu
NR_003085.2:n.1491C>T
XM_006715742.2:c.1403C>T XP_006715805.1:p.Pro468Leu
XM_006715744.2:c.476C>T XP_006715807.1:p.Pro159Leu
XM_011515427.1:c.1454C>T XP_011513729.1:p.Pro485Leu
XM_011515428.1:c.1298C>T XP_011513730.1:p.Pro433Leu
XM_011515429.1:c.1091C>T XP_011513731.1:p.Pro364Leu
XM_011515430.1:c.1091C>T XP_011513732.1:p.Pro364Leu
NM_000535.6:c.1409C>T NP_000526.2:p.Pro470Leu
NM_001322003.1:c.1004C>T NP_001308932.1:p.Pro335Leu
NM_001322004.1:c.1004C>T NP_001308933.1:p.Pro335Leu
NM_001322005.1:c.1004C>T NP_001308934.1:p.Pro335Leu
NM_001322006.1:c.1253C>T NP_001308935.1:p.Pro418Leu
NM_001322007.1:c.1091C>T NP_001308936.1:p.Pro364Leu
NM_001322008.1:c.1091C>T NP_001308937.1:p.Pro364Leu
NM_001322009.1:c.1004C>T NP_001308938.1:p.Pro335Leu
NM_001322010.1:c.848C>T NP_001308939.1:p.Pro283Leu
NM_001322011.1:c.476C>T NP_001308940.1:p.Pro159Leu
NM_001322012.1:c.476C>T NP_001308941.1:p.Pro159Leu
NM_001322013.1:c.836C>T NP_001308942.1:p.Pro279Leu
NM_001322014.1:c.1409C>T NP_001308943.1:p.Pro470Leu
NM_001322015.1:c.1100C>T NP_001308944.1:p.Pro367Leu
NR_136154.1:n.1496C>T
XM_006715744.4:c.476C>T XP_006715807.1:p.Pro159Leu
XM_017012342.2:c.476C>T XP_016867831.1:p.Pro159Leu
XM_024446800.1:c.848C>T XP_024302568.1:p.Pro283Leu
NM_000535.7:c.1409C>T MANE Select NP_000526.2:p.Pro470Leu
NM_001322003.2:c.1004C>T NP_001308932.1:p.Pro335Leu
NM_001322004.2:c.1004C>T NP_001308933.1:p.Pro335Leu
NM_001322005.2:c.1004C>T NP_001308934.1:p.Pro335Leu
NM_001322006.2:c.1253C>T NP_001308935.1:p.Pro418Leu
NM_001322008.2:c.1091C>T NP_001308937.1:p.Pro364Leu
NM_001322009.2:c.1004C>T NP_001308938.1:p.Pro335Leu
NM_001322010.2:c.848C>T NP_001308939.1:p.Pro283Leu
NM_001322011.2:c.476C>T NP_001308940.1:p.Pro159Leu
NM_001322012.2:c.476C>T NP_001308941.1:p.Pro159Leu
NM_001322013.2:c.836C>T NP_001308942.1:p.Pro279Leu
NM_001322014.2:c.1409C>T NP_001308943.1:p.Pro470Leu
NM_001322015.2:c.1100C>T NP_001308944.1:p.Pro367Leu
NM_001322007.2:c.1091C>T NP_001308936.1:p.Pro364Leu