Canonical Allele Identifier: CA2658946266

Gene: MSH2

Linked Data

• gnomAD v4: 2-47412607-G-GTAATATA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47412613_47412619dup , CM000664.2:g.47412613_47412619dup	GRCh38
NC_000002.11:g.47639752_47639758dup , CM000664.1:g.47639752_47639758dup	GRCh37
NC_000002.10:g.47493256_47493262dup	NCBI36
NG_007110.2:g.14490_14496dup , LRG_218:g.14490_14496dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.792+53_792+59dup	ENSP00000495641.2:n.792+53_792+59dup
ENST00000233146.7:c.792+53_792+59dup MANE Select	ENSP00000233146.2:n.792+53_792+59dup
ENST00000543555.6:c.594+53_594+59dup	ENSP00000442697.1:n.594+53_594+59dup
ENST00000644092.1:c.792+53_792+59dup	ENSP00000496351.1:n.792+53_792+59dup
ENST00000645339.1:c.792+53_792+59dup	ENSP00000496441.1:n.792+53_792+59dup
ENST00000645506.1:c.792+53_792+59dup	ENSP00000495455.1:n.792+53_792+59dup
ENST00000646415.1:c.792+53_792+59dup	ENSP00000495543.1:n.792+53_792+59dup
ENST00000233146.6:c.792+53_792+59dup	ENSP00000233146.2:n.792+53_792+59dup
ENST00000406134.5:c.792+53_792+59dup	ENSP00000384199.1:n.792+53_792+59dup
ENST00000543555.5:c.594+53_594+59dup	ENSP00000442697.1:n.594+53_594+59dup
ENST00000610696.4:c.792+53_792+59dup	ENSP00000483159.1:n.792+53_792+59dup
ENST00000613514.4:c.792+53_792+59dup	ENSP00000484137.1:n.792+53_792+59dup
ENST00000617333.3:c.792+53_792+59dup	ENSP00000482468.1:n.792+53_792+59dup
ENST00000617938.4:c.792+53_792+59dup	ENSP00000481158.1:n.792+53_792+59dup
ENST00000621359.2:c.792+53_792+59dup	ENSP00000481416.1:n.792+53_792+59dup
NM_000251.2:c.792+53_792+59dup , LRG_218t1:c.792+53_792+59dup	NP_000242.1:n.792+53_792+59dup
NM_001258281.1:c.594+53_594+59dup	NP_001245210.1:n.594+53_594+59dup
XM_005264332.2:c.792+53_792+59dup	XP_005264389.2:n.792+53_792+59dup
XM_011532867.1:c.792+53_792+59dup	XP_011531169.1:n.792+53_792+59dup
XR_939685.1:n.864+53_864+59dup
XM_005264332.4:c.792+53_792+59dup	XP_005264389.2:n.792+53_792+59dup
XM_011532867.2:c.792+53_792+59dup	XP_011531169.1:n.792+53_792+59dup
XR_001738747.2:n.854+53_854+59dup
XR_939685.2:n.854+53_854+59dup
NM_000251.3:c.792+53_792+59dup MANE Select	NP_000242.1:n.792+53_792+59dup