Canonical Allele Identifier: CA366739673

Gene: PMS2

Linked Data

• ClinVar Variation Id: 455672
• ClinVar RCV Id: RCV000532591 ; RCV000581381
• dbSNP Id: rs1554297188
• COSMIC: COSM1221329
• MyVariant Identifiers: chr7:g.6026563A>C (hg19) ; chr7:g.5986932A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5986932A>C , CM000669.2:g.5986932A>C	GRCh38
NC_000007.13:g.6026563A>C , CM000669.1:g.6026563A>C	GRCh37
NC_000007.12:g.5993089A>C	NCBI36
NG_008466.1:g.27175T>G , LRG_161:g.27175T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699814.2:c.*1229T>G	ENSP00000514615.2:n.*1229T>G
ENST00000699840.2:c.1830T>G	ENSP00000514638.2:p.Ile610Met
ENST00000699930.2:c.1725T>G	ENSP00000514695.2:p.Ile575Met
ENST00000406569.8:c.1678+155T>G	ENSP00000514464.1:n.1678+155T>G
ENST00000644110.2:c.*1427T>G	ENSP00000496392.2:n.*1427T>G
ENST00000699752.1:c.1677T>G	ENSP00000514561.1:p.Ile559Met
ENST00000699753.1:c.*1254T>G	ENSP00000514562.1:n.*1254T>G
ENST00000699754.1:c.1635T>G	ENSP00000514563.1:p.Ile545Met
ENST00000699755.1:c.*1232T>G	ENSP00000514564.1:n.*1232T>G
ENST00000699756.1:c.*1420T>G	ENSP00000514565.1:n.*1420T>G
ENST00000699757.1:c.*1090T>G	ENSP00000514566.1:n.*1090T>G
ENST00000699758.1:c.*1090T>G	ENSP00000514567.1:n.*1090T>G
ENST00000699759.1:n.2687T>G
ENST00000699760.1:c.1515T>G	ENSP00000514568.1:p.Ile505Met
ENST00000699761.1:c.1428T>G	ENSP00000514569.1:p.Ile476Met
ENST00000699762.1:c.1260T>G	ENSP00000514570.1:p.Ile420Met
ENST00000699763.1:c.*923T>G	ENSP00000514571.1:n.*923T>G
ENST00000699764.1:c.*151T>G	ENSP00000514572.1:n.*151T>G
ENST00000699765.1:c.*929T>G	ENSP00000514573.1:n.*929T>G
ENST00000699766.1:c.1833T>G	ENSP00000514574.1:p.Ile611Met
ENST00000699767.1:c.1833T>G	ENSP00000514575.1:p.Ile611Met
ENST00000699768.1:c.1833T>G	ENSP00000514576.1:p.Ile611Met
ENST00000699811.1:c.1428T>G	ENSP00000514614.1:p.Ile476Met
ENST00000699813.1:n.1946T>G
ENST00000699814.1:c.1456T>G
ENST00000699815.1:c.*1364T>G	ENSP00000514616.1:n.*1364T>G
ENST00000699816.1:c.*723T>G	ENSP00000514617.1:n.*723T>G
ENST00000699817.1:c.*1427T>G	ENSP00000514618.1:n.*1427T>G
ENST00000699818.1:c.1428T>G	ENSP00000514619.1:p.Ile476Met
ENST00000699819.1:c.*990T>G	ENSP00000514620.1:n.*990T>G
ENST00000699820.1:c.1144+2868T>G	ENSP00000514621.1:n.1144+2868T>G
ENST00000699821.1:c.1428T>G	ENSP00000514622.1:p.Ile476Met
ENST00000699822.1:c.*1285T>G	ENSP00000514623.1:n.*1285T>G
ENST00000699823.1:c.1428T>G	ENSP00000514624.1:p.Ile476Met
ENST00000699824.1:c.*1336T>G	ENSP00000514625.1:n.*1336T>G
ENST00000699825.1:c.1272T>G	ENSP00000514626.1:p.Ile424Met
ENST00000699826.1:c.*1232T>G	ENSP00000514627.1:n.*1232T>G
ENST00000699827.1:c.1665T>G	ENSP00000514628.1:p.Ile555Met
ENST00000699828.1:c.*923T>G	ENSP00000514629.1:n.*923T>G
ENST00000699833.1:n.3605T>G
ENST00000699837.1:c.1428T>G	ENSP00000514635.1:p.Ile476Met
ENST00000699838.1:c.*1733T>G	ENSP00000514636.1:n.*1733T>G
ENST00000699839.1:c.2019T>G	ENSP00000514637.1:p.Ile673Met
ENST00000699916.1:c.*1090T>G	ENSP00000514684.1:n.*1090T>G
ENST00000699917.1:c.*1282T>G	ENSP00000514685.1:n.*1282T>G
ENST00000699918.1:c.*1334T>G	ENSP00000514686.1:n.*1334T>G
ENST00000699919.1:c.*1420T>G	ENSP00000514687.1:n.*1420T>G
ENST00000699920.1:c.*1469T>G	ENSP00000514688.1:n.*1469T>G
ENST00000699928.1:c.989-3941T>G	ENSP00000514693.1:n.989-3941T>G
ENST00000699951.1:c.*929T>G	ENSP00000514706.1:n.*929T>G
ENST00000699952.1:c.803+10394T>G	ENSP00000514707.1:n.803+10394T>G
ENST00000265849.12:c.1833T>G MANE Select	ENSP00000265849.7:p.Ile611Met
ENST00000642292.1:c.1428T>G	ENSP00000495524.1:p.Ile476Met
ENST00000642456.1:c.1428T>G	ENSP00000493814.1:p.Ile476Met
ENST00000643595.1:c.*1232T>G	ENSP00000494497.1:n.*1232T>G
ENST00000644110.1:c.1515T>G	ENSP00000496392.1:p.Ile505Met
ENST00000265849.11:c.1833T>G	ENSP00000265849.7:p.Ile611Met
ENST00000382321.5:c.804-3941T>G	ENSP00000371758.4:n.804-3941T>G
ENST00000406569.7:n.1678+155T>G
ENST00000441476.6:c.1515T>G	ENSP00000392843.2:p.Ile505Met
ENST00000469652.1:n.63-4027T>G
NM_000535.5:c.1833T>G , LRG_161t1:c.1833T>G	NP_000526.1:p.Ile611Met
NR_003085.2:n.1915T>G
XM_006715742.2:c.1827T>G	XP_006715805.1:p.Ile609Met
XM_006715744.2:c.900T>G	XP_006715807.1:p.Ile300Met
XM_011515427.1:c.1878T>G	XP_011513729.1:p.Ile626Met
XM_011515428.1:c.1722T>G	XP_011513730.1:p.Ile574Met
XM_011515429.1:c.1515T>G	XP_011513731.1:p.Ile505Met
XM_011515430.1:c.1515T>G	XP_011513732.1:p.Ile505Met
NM_000535.6:c.1833T>G	NP_000526.2:p.Ile611Met
NM_001322003.1:c.1428T>G	NP_001308932.1:p.Ile476Met
NM_001322004.1:c.1428T>G	NP_001308933.1:p.Ile476Met
NM_001322005.1:c.1428T>G	NP_001308934.1:p.Ile476Met
NM_001322006.1:c.1677T>G	NP_001308935.1:p.Ile559Met
NM_001322007.1:c.1515T>G	NP_001308936.1:p.Ile505Met
NM_001322008.1:c.1515T>G	NP_001308937.1:p.Ile505Met
NM_001322009.1:c.1428T>G	NP_001308938.1:p.Ile476Met
NM_001322010.1:c.1272T>G	NP_001308939.1:p.Ile424Met
NM_001322011.1:c.900T>G	NP_001308940.1:p.Ile300Met
NM_001322012.1:c.900T>G	NP_001308941.1:p.Ile300Met
NM_001322013.1:c.1260T>G	NP_001308942.1:p.Ile420Met
NM_001322014.1:c.1833T>G	NP_001308943.1:p.Ile611Met
NM_001322015.1:c.1524T>G	NP_001308944.1:p.Ile508Met
NR_136154.1:n.1920T>G
XM_006715744.4:c.900T>G	XP_006715807.1:p.Ile300Met
XM_017012342.2:c.900T>G	XP_016867831.1:p.Ile300Met
XM_024446800.1:c.1272T>G	XP_024302568.1:p.Ile424Met
NM_000535.7:c.1833T>G MANE Select	NP_000526.2:p.Ile611Met
NM_001322003.2:c.1428T>G	NP_001308932.1:p.Ile476Met
NM_001322004.2:c.1428T>G	NP_001308933.1:p.Ile476Met
NM_001322005.2:c.1428T>G	NP_001308934.1:p.Ile476Met
NM_001322006.2:c.1677T>G	NP_001308935.1:p.Ile559Met
NM_001322008.2:c.1515T>G	NP_001308937.1:p.Ile505Met
NM_001322009.2:c.1428T>G	NP_001308938.1:p.Ile476Met
NM_001322010.2:c.1272T>G	NP_001308939.1:p.Ile424Met
NM_001322011.2:c.900T>G	NP_001308940.1:p.Ile300Met
NM_001322012.2:c.900T>G	NP_001308941.1:p.Ile300Met
NM_001322013.2:c.1260T>G	NP_001308942.1:p.Ile420Met
NM_001322014.2:c.1833T>G	NP_001308943.1:p.Ile611Met
NM_001322015.2:c.1524T>G	NP_001308944.1:p.Ile508Met
NM_001322007.2:c.1515T>G	NP_001308936.1:p.Ile505Met