Canonical Allele Identifier: CA009239
Gene: PMS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91291
dbSNP Id: rs267608158

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5989798A>T , CM000669.2:g.5989798A>T GRCh38
NC_000007.13:g.6029429A>T , CM000669.1:g.6029429A>T GRCh37
NC_000007.12:g.5995955A>T NCBI36
NG_008466.1:g.24309T>A , LRG_161:g.24309T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265849.12:c.1144+2T>A MANE Select ENSP00000265849.7:p.=
ENST00000642292.1:c.739+2T>A ENSP00000495524.1:p.=
ENST00000642456.1:c.739+2T>A ENSP00000493814.1:p.=
ENST00000643595.1:c.*543+2T>A ENSP00000494497.1:p.=
ENST00000644110.1:n.826+2T>A ENSP00000496392.1:p.=
ENST00000265849.11:c.1144+2T>A ENSP00000265849.7:p.=
ENST00000382321.5:n.804-6807T>A ENSP00000371758.4:p.=
ENST00000406569.7:n.1144+2T>A
ENST00000441476.6:c.826+2T>A ENSP00000392843.2:p.=
ENST00000469652.1:n.63-6893T>A
NM_000535.5:c.1144+2T>A , LRG_161t1:c.1144+2T>A NP_000526.1:p.=
NR_003085.2:n.1226+2T>A
XM_006715742.2:c.1138+2T>A XP_006715805.1:p.=
XM_006715744.2:c.211+2T>A XP_006715807.1:p.=
XM_011515427.1:c.1189+2T>A XP_011513729.1:p.=
XM_011515428.1:c.1033+2175T>A XP_011513730.1:p.=
XM_011515429.1:c.826+2T>A XP_011513731.1:p.=
XM_011515430.1:c.826+2T>A XP_011513732.1:p.=
NM_000535.6:c.1144+2T>A NP_000526.2:p.=
NM_001322003.1:c.739+2T>A NP_001308932.1:p.=
NM_001322004.1:c.739+2T>A NP_001308933.1:p.=
NM_001322005.1:c.739+2T>A NP_001308934.1:p.=
NM_001322006.1:c.988+2175T>A NP_001308935.1:p.=
NM_001322007.1:c.826+2T>A NP_001308936.1:p.=
NM_001322008.1:c.826+2T>A NP_001308937.1:p.=
NM_001322009.1:c.739+2T>A NP_001308938.1:p.=
NM_001322010.1:c.583+2175T>A NP_001308939.1:p.=
NM_001322011.1:c.211+2T>A NP_001308940.1:p.=
NM_001322012.1:c.211+2T>A NP_001308941.1:p.=
NM_001322013.1:c.571+2T>A NP_001308942.1:p.=
NM_001322014.1:c.1144+2T>A NP_001308943.1:p.=
NM_001322015.1:c.835+2T>A NP_001308944.1:p.=
NR_136154.1:n.1231+2T>A
XM_006715744.4:c.211+2T>A XP_006715807.1:p.=
XM_017012342.2:c.211+2T>A XP_016867831.1:p.=
XM_024446800.1:c.583+2175T>A XP_024302568.1:p.=
NM_000535.7:c.1144+2T>A MANE Select NP_000526.2:p.=
NM_001322003.2:c.739+2T>A NP_001308932.1:p.=
NM_001322004.2:c.739+2T>A NP_001308933.1:p.=
NM_001322005.2:c.739+2T>A NP_001308934.1:p.=
NM_001322006.2:c.988+2175T>A NP_001308935.1:p.=
NM_001322008.2:c.826+2T>A NP_001308937.1:p.=
NM_001322009.2:c.739+2T>A NP_001308938.1:p.=
NM_001322010.2:c.583+2175T>A NP_001308939.1:p.=
NM_001322011.2:c.211+2T>A NP_001308940.1:p.=
NM_001322012.2:c.211+2T>A NP_001308941.1:p.=
NM_001322013.2:c.571+2T>A NP_001308942.1:p.=
NM_001322014.2:c.1144+2T>A NP_001308943.1:p.=
NM_001322015.2:c.835+2T>A NP_001308944.1:p.=
NM_001322007.2:c.826+2T>A NP_001308936.1:p.=