Canonical Allele Identifier: CA2658944990

Gene: MSH2

Linked Data

• gnomAD v4: 2-47403432-G-GGGACCCGGGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403433_47403444dup , CM000664.2:g.47403433_47403444dup	GRCh38
NC_000002.11:g.47630572_47630583dup , CM000664.1:g.47630572_47630583dup	GRCh37
NC_000002.10:g.47484076_47484087dup	NCBI36
NG_007110.2:g.5310_5321dup , LRG_218:g.5310_5321dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.211+31_211+42dup	ENSP00000495641.2:n.211+31_211+42dup
ENST00000233146.7:c.211+31_211+42dup MANE Select	ENSP00000233146.2:n.211+31_211+42dup
ENST00000543555.6:c.13+31_13+42dup	ENSP00000442697.1:n.13+31_13+42dup
ENST00000644092.1:c.211+31_211+42dup	ENSP00000496351.1:n.211+31_211+42dup
ENST00000645339.1:c.211+31_211+42dup	ENSP00000496441.1:n.211+31_211+42dup
ENST00000645506.1:c.211+31_211+42dup	ENSP00000495455.1:n.211+31_211+42dup
ENST00000646415.1:c.211+31_211+42dup	ENSP00000495543.1:n.211+31_211+42dup
ENST00000233146.6:c.211+31_211+42dup	ENSP00000233146.2:n.211+31_211+42dup
ENST00000406134.5:c.211+31_211+42dup	ENSP00000384199.1:n.211+31_211+42dup
ENST00000454849.5:c.13+31_13+42dup	ENSP00000411482.1:n.13+31_13+42dup
ENST00000543555.5:c.13+31_13+42dup	ENSP00000442697.1:n.13+31_13+42dup
ENST00000610696.4:c.211+31_211+42dup	ENSP00000483159.1:n.211+31_211+42dup
ENST00000613514.4:c.211+31_211+42dup	ENSP00000484137.1:n.211+31_211+42dup
ENST00000617333.3:c.211+31_211+42dup	ENSP00000482468.1:n.211+31_211+42dup
ENST00000617938.4:c.211+31_211+42dup	ENSP00000481158.1:n.211+31_211+42dup
ENST00000621359.2:c.211+31_211+42dup	ENSP00000481416.1:n.211+31_211+42dup
NM_000251.2:c.211+31_211+42dup , LRG_218t1:c.211+31_211+42dup	NP_000242.1:n.211+31_211+42dup
NM_001258281.1:c.13+31_13+42dup	NP_001245210.1:n.13+31_13+42dup
XM_005264332.2:c.211+31_211+42dup	XP_005264389.2:n.211+31_211+42dup
XM_011532867.1:c.211+31_211+42dup	XP_011531169.1:n.211+31_211+42dup
XR_939685.1:n.283+31_283+42dup
XM_005264332.4:c.211+31_211+42dup	XP_005264389.2:n.211+31_211+42dup
XM_011532867.2:c.211+31_211+42dup	XP_011531169.1:n.211+31_211+42dup
XR_001738747.2:n.273+31_273+42dup
XR_939685.2:n.273+31_273+42dup
NM_000251.3:c.211+31_211+42dup MANE Select	NP_000242.1:n.211+31_211+42dup