Canonical Allele Identifier: CA2495843953

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47430222_47430223delinsAT , CM000664.2:g.47430222_47430223delinsAT	GRCh38
NC_000002.11:g.47657361_47657362delinsAT , CM000664.1:g.47657361_47657362delinsAT	GRCh37
NC_000002.10:g.47510865_47510866delinsAT	NCBI36
NG_007110.2:g.32099_32100delinsAT , LRG_218:g.32099_32100delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1276+281_1276+282delinsAT	ENSP00000495641.2:n.1276+281_1276+282delinsAT
ENST00000233146.7:c.1276+281_1276+282delinsAT MANE Select	ENSP00000233146.2:n.1276+281_1276+282delinsAT
ENST00000543555.6:c.1078+281_1078+282delinsAT	ENSP00000442697.1:n.1078+281_1078+282delinsAT
ENST00000644092.1:c.1276+281_1276+282delinsAT	ENSP00000496351.1:n.1276+281_1276+282delinsAT
ENST00000645339.1:c.1276+281_1276+282delinsAT	ENSP00000496441.1:n.1276+281_1276+282delinsAT
ENST00000645506.1:c.1276+281_1276+282delinsAT	ENSP00000495455.1:n.1276+281_1276+282delinsAT
ENST00000646415.1:c.1276+281_1276+282delinsAT	ENSP00000495543.1:n.1276+281_1276+282delinsAT
ENST00000233146.6:c.1276+281_1276+282delinsAT	ENSP00000233146.2:n.1276+281_1276+282delinsAT
ENST00000406134.5:c.1276+281_1276+282delinsAT	ENSP00000384199.1:n.1276+281_1276+282delinsAT
ENST00000543555.5:c.1078+281_1078+282delinsAT	ENSP00000442697.1:n.1078+281_1078+282delinsAT
ENST00000610696.4:c.1276+281_1276+282delinsAT	ENSP00000483159.1:n.1276+281_1276+282delinsAT
ENST00000613514.4:c.1276+281_1276+282delinsAT	ENSP00000484137.1:n.1276+281_1276+282delinsAT
ENST00000617333.3:c.*42+281_*42+282delinsAT	ENSP00000482468.1:n.*42+281_*42+282delinsAT
ENST00000617938.4:c.*248+281_*248+282delinsAT	ENSP00000481158.1:n.*248+281_*248+282delinsAT
ENST00000621359.2:c.1276+281_1276+282delinsAT	ENSP00000481416.1:n.1276+281_1276+282delinsAT
NM_000251.2:c.1276+281_1276+282delinsAT , LRG_218t1:c.1276+281_1276+282delinsAT	NP_000242.1:n.1276+281_1276+282delinsAT
NM_001258281.1:c.1078+281_1078+282delinsAT	NP_001245210.1:n.1078+281_1078+282delinsAT
XM_005264332.2:c.1276+281_1276+282delinsAT	XP_005264389.2:n.1276+281_1276+282delinsAT
XM_011532867.1:c.1276+281_1276+282delinsAT	XP_011531169.1:n.1276+281_1276+282delinsAT
XR_939685.1:n.1348+281_1348+282delinsAT
XM_005264332.4:c.1276+281_1276+282delinsAT	XP_005264389.2:n.1276+281_1276+282delinsAT
XM_011532867.2:c.1276+281_1276+282delinsAT	XP_011531169.1:n.1276+281_1276+282delinsAT
XR_001738747.2:n.1338+281_1338+282delinsAT
XR_939685.2:n.1338+281_1338+282delinsAT
NM_000251.3:c.1276+281_1276+282delinsAT MANE Select	NP_000242.1:n.1276+281_1276+282delinsAT