Canonical Allele Identifier: CA2495873333
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47476647_47476648delinsAT , CM000664.2:g.47476647_47476648delinsAT GRCh38
NC_000002.11:g.47703786_47703787delinsAT , CM000664.1:g.47703786_47703787delinsAT GRCh37
NC_000002.10:g.47557290_47557291delinsAT NCBI36
NG_007110.2:g.78524_78525delinsAT , LRG_218:g.78524_78525delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.2210+76_2210+77delinsAT ENSP00000495641.2:n.2210+76_2210+77delinsAT
ENST00000233146.7:c.2210+76_2210+77delinsAT MANE Select ENSP00000233146.2:n.2210+76_2210+77delinsAT
ENST00000543555.6:c.2012+76_2012+77delinsAT ENSP00000442697.1:n.2012+76_2012+77delinsAT
ENST00000644092.1:c.*510+76_*510+77delinsAT ENSP00000496351.1:n.*510+76_*510+77delinsAT
ENST00000644900.1:c.63+76_63+77delinsAT
ENST00000645339.1:c.2210+76_2210+77delinsAT ENSP00000496441.1:n.2210+76_2210+77delinsAT
ENST00000645506.1:c.2210+76_2210+77delinsAT ENSP00000495455.1:n.2210+76_2210+77delinsAT
ENST00000646415.1:c.2210+76_2210+77delinsAT ENSP00000495543.1:n.2210+76_2210+77delinsAT
ENST00000233146.6:c.2210+76_2210+77delinsAT ENSP00000233146.2:n.2210+76_2210+77delinsAT
ENST00000406134.5:c.2210+76_2210+77delinsAT ENSP00000384199.1:n.2210+76_2210+77delinsAT
ENST00000543555.5:c.2012+76_2012+77delinsAT ENSP00000442697.1:n.2012+76_2012+77delinsAT
ENST00000610696.4:c.*606+76_*606+77delinsAT ENSP00000483159.1:n.*606+76_*606+77delinsAT
ENST00000613514.4:c.*750+76_*750+77delinsAT ENSP00000484137.1:n.*750+76_*750+77delinsAT
ENST00000617333.3:c.*976+76_*976+77delinsAT ENSP00000482468.1:n.*976+76_*976+77delinsAT
ENST00000617938.4:c.*1182+76_*1182+77delinsAT ENSP00000481158.1:n.*1182+76_*1182+77delinsAT
ENST00000621359.2:c.2210+76_2210+77delinsAT ENSP00000481416.1:n.2210+76_2210+77delinsAT
NM_000251.2:c.2210+76_2210+77delinsAT , LRG_218t1:c.2210+76_2210+77delinsAT NP_000242.1:n.2210+76_2210+77delinsAT
NM_001258281.1:c.2012+76_2012+77delinsAT NP_001245210.1:n.2012+76_2012+77delinsAT
XM_005264332.2:c.2210+76_2210+77delinsAT XP_005264389.2:n.2210+76_2210+77delinsAT
XM_011532867.1:c.2210+76_2210+77delinsAT XP_011531169.1:n.2210+76_2210+77delinsAT
XR_939685.1:n.2282+76_2282+77delinsAT
XM_005264332.4:c.2210+76_2210+77delinsAT XP_005264389.2:n.2210+76_2210+77delinsAT
XM_011532867.2:c.2210+76_2210+77delinsAT XP_011531169.1:n.2210+76_2210+77delinsAT
XR_001738747.2:n.2272+76_2272+77delinsAT
XR_939685.2:n.2272+76_2272+77delinsAT
NM_000251.3:c.2210+76_2210+77delinsAT MANE Select NP_000242.1:n.2210+76_2210+77delinsAT