Canonical Allele Identifier: CA2495832840

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47412619_47412622delinsAAAT , CM000664.2:g.47412619_47412622delinsAAAT	GRCh38
NC_000002.11:g.47639758_47639761delinsAAAT , CM000664.1:g.47639758_47639761delinsAAAT	GRCh37
NC_000002.10:g.47493262_47493265delinsAAAT	NCBI36
NG_007110.2:g.14496_14499delinsAAAT , LRG_218:g.14496_14499delinsAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.792+59_792+62delinsAAAT	ENSP00000495641.2:n.792+59_792+62delinsAAAT
ENST00000233146.7:c.792+59_792+62delinsAAAT MANE Select	ENSP00000233146.2:n.792+59_792+62delinsAAAT
ENST00000543555.6:c.594+59_594+62delinsAAAT	ENSP00000442697.1:n.594+59_594+62delinsAAAT
ENST00000644092.1:c.792+59_792+62delinsAAAT	ENSP00000496351.1:n.792+59_792+62delinsAAAT
ENST00000645339.1:c.792+59_792+62delinsAAAT	ENSP00000496441.1:n.792+59_792+62delinsAAAT
ENST00000645506.1:c.792+59_792+62delinsAAAT	ENSP00000495455.1:n.792+59_792+62delinsAAAT
ENST00000646415.1:c.792+59_792+62delinsAAAT	ENSP00000495543.1:n.792+59_792+62delinsAAAT
ENST00000233146.6:c.792+59_792+62delinsAAAT	ENSP00000233146.2:n.792+59_792+62delinsAAAT
ENST00000406134.5:c.792+59_792+62delinsAAAT	ENSP00000384199.1:n.792+59_792+62delinsAAAT
ENST00000543555.5:c.594+59_594+62delinsAAAT	ENSP00000442697.1:n.594+59_594+62delinsAAAT
ENST00000610696.4:c.792+59_792+62delinsAAAT	ENSP00000483159.1:n.792+59_792+62delinsAAAT
ENST00000613514.4:c.792+59_792+62delinsAAAT	ENSP00000484137.1:n.792+59_792+62delinsAAAT
ENST00000617333.3:c.792+59_792+62delinsAAAT	ENSP00000482468.1:n.792+59_792+62delinsAAAT
ENST00000617938.4:c.792+59_792+62delinsAAAT	ENSP00000481158.1:n.792+59_792+62delinsAAAT
ENST00000621359.2:c.792+59_792+62delinsAAAT	ENSP00000481416.1:n.792+59_792+62delinsAAAT
NM_000251.2:c.792+59_792+62delinsAAAT , LRG_218t1:c.792+59_792+62delinsAAAT	NP_000242.1:n.792+59_792+62delinsAAAT
NM_001258281.1:c.594+59_594+62delinsAAAT	NP_001245210.1:n.594+59_594+62delinsAAAT
XM_005264332.2:c.792+59_792+62delinsAAAT	XP_005264389.2:n.792+59_792+62delinsAAAT
XM_011532867.1:c.792+59_792+62delinsAAAT	XP_011531169.1:n.792+59_792+62delinsAAAT
XR_939685.1:n.864+59_864+62delinsAAAT
XM_005264332.4:c.792+59_792+62delinsAAAT	XP_005264389.2:n.792+59_792+62delinsAAAT
XM_011532867.2:c.792+59_792+62delinsAAAT	XP_011531169.1:n.792+59_792+62delinsAAAT
XR_001738747.2:n.854+59_854+62delinsAAAT
XR_939685.2:n.854+59_854+62delinsAAAT
NM_000251.3:c.792+59_792+62delinsAAAT MANE Select	NP_000242.1:n.792+59_792+62delinsAAAT