Canonical Allele Identifier: CA2658946850

Gene: MSH2

Linked Data

• gnomAD v4: 2-47429661-A-AGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47429663_47429665dup , CM000664.2:g.47429663_47429665dup	GRCh38
NC_000002.11:g.47656802_47656804dup , CM000664.1:g.47656802_47656804dup	GRCh37
NC_000002.10:g.47510306_47510308dup	NCBI36
NG_007110.2:g.31540_31542dup , LRG_218:g.31540_31542dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1077-79_1077-77dup	ENSP00000495641.2:n.1077-79_1077-77dup
ENST00000233146.7:c.1077-79_1077-77dup MANE Select	ENSP00000233146.2:n.1077-79_1077-77dup
ENST00000543555.6:c.879-79_879-77dup	ENSP00000442697.1:n.879-79_879-77dup
ENST00000644092.1:c.1077-79_1077-77dup	ENSP00000496351.1:n.1077-79_1077-77dup
ENST00000645339.1:c.1077-79_1077-77dup	ENSP00000496441.1:n.1077-79_1077-77dup
ENST00000645506.1:c.1077-79_1077-77dup	ENSP00000495455.1:n.1077-79_1077-77dup
ENST00000646415.1:c.1077-79_1077-77dup	ENSP00000495543.1:n.1077-79_1077-77dup
ENST00000233146.6:c.1077-79_1077-77dup	ENSP00000233146.2:n.1077-79_1077-77dup
ENST00000406134.5:c.1077-79_1077-77dup	ENSP00000384199.1:n.1077-79_1077-77dup
ENST00000543555.5:c.879-79_879-77dup	ENSP00000442697.1:n.879-79_879-77dup
ENST00000610696.4:c.1077-79_1077-77dup	ENSP00000483159.1:n.1077-79_1077-77dup
ENST00000613514.4:c.1077-79_1077-77dup	ENSP00000484137.1:n.1077-79_1077-77dup
ENST00000617333.3:c.1077-79_1077-77dup	ENSP00000482468.1:n.1077-79_1077-77dup
ENST00000617938.4:c.*49-79_*49-77dup	ENSP00000481158.1:n.*49-79_*49-77dup
ENST00000621359.2:c.1077-79_1077-77dup	ENSP00000481416.1:n.1077-79_1077-77dup
NM_000251.2:c.1077-79_1077-77dup , LRG_218t1:c.1077-79_1077-77dup	NP_000242.1:n.1077-79_1077-77dup
NM_001258281.1:c.879-79_879-77dup	NP_001245210.1:n.879-79_879-77dup
XM_005264332.2:c.1077-79_1077-77dup	XP_005264389.2:n.1077-79_1077-77dup
XM_011532867.1:c.1077-79_1077-77dup	XP_011531169.1:n.1077-79_1077-77dup
XR_939685.1:n.1149-79_1149-77dup
XM_005264332.4:c.1077-79_1077-77dup	XP_005264389.2:n.1077-79_1077-77dup
XM_011532867.2:c.1077-79_1077-77dup	XP_011531169.1:n.1077-79_1077-77dup
XR_001738747.2:n.1139-79_1139-77dup
XR_939685.2:n.1139-79_1139-77dup
NM_000251.3:c.1077-79_1077-77dup MANE Select	NP_000242.1:n.1077-79_1077-77dup