Canonical Allele Identifier: CA2495876050

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480741_47480742delinsAT , CM000664.2:g.47480741_47480742delinsAT	GRCh38
NC_000002.11:g.47707880_47707881delinsAT , CM000664.1:g.47707880_47707881delinsAT	GRCh37
NC_000002.10:g.47561384_47561385delinsAT	NCBI36
NG_007110.2:g.82618_82619delinsAT , LRG_218:g.82618_82619delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2504_2505delinsAT	ENSP00000495641.2:p.Asn835=
ENST00000233146.7:c.2504_2505delinsAT MANE Select	ENSP00000233146.2:p.Asn835=
ENST00000543555.6:c.2306_2307delinsAT	ENSP00000442697.1:p.Asn769=
ENST00000644092.1:c.*804_*805delinsAT	ENSP00000496351.1:n.*804_*805delinsAT
ENST00000644900.1:c.357_358delinsAT
ENST00000645339.1:c.2504_2505delinsAT	ENSP00000496441.1:p.Asn835=
ENST00000645506.1:c.2504_2505delinsAT	ENSP00000495455.1:p.Asn835=
ENST00000646415.1:c.2504_2505delinsAT	ENSP00000495543.1:p.Asn835=
ENST00000233146.6:c.2504_2505delinsAT	ENSP00000233146.2:p.Asn835=
ENST00000406134.5:c.2504_2505delinsAT	ENSP00000384199.1:p.Asn835=
ENST00000543555.5:c.2306_2307delinsAT	ENSP00000442697.1:p.Asn769=
ENST00000610696.4:c.*900_*901delinsAT	ENSP00000483159.1:n.*900_*901delinsAT
ENST00000613514.4:c.*1044_*1045delinsAT	ENSP00000484137.1:n.*1044_*1045delinsAT
ENST00000617333.3:c.*1270_*1271delinsAT	ENSP00000482468.1:n.*1270_*1271delinsAT
ENST00000617938.4:c.*1476_*1477delinsAT	ENSP00000481158.1:n.*1476_*1477delinsAT
ENST00000621359.2:c.*70_*71delinsAT	ENSP00000481416.1:n.*70_*71delinsAT
NM_000251.2:c.2504_2505delinsAT , LRG_218t1:c.2504_2505delinsAT	NP_000242.1:p.Asn835=
NM_001258281.1:c.2306_2307delinsAT	NP_001245210.1:p.Asn769=
XM_005264332.2:c.2504_2505delinsAT	XP_005264389.2:p.Asn835=
XM_011532867.1:c.2504_2505delinsAT	XP_011531169.1:p.Asn835=
XR_939685.1:n.2576_2577delinsAT
XM_005264332.4:c.2504_2505delinsAT	XP_005264389.2:p.Asn835=
XM_011532867.2:c.2504_2505delinsAT	XP_011531169.1:p.Asn835=
XR_001738747.2:n.2566_2567delinsAT
XR_939685.2:n.2566_2567delinsAT
NM_000251.3:c.2504_2505delinsAT MANE Select	NP_000242.1:p.Asn835=