Canonical Allele Identifier: CA2495826392

Gene: MSH2

Linked Data

• dbSNP Id: rs1672215494

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403067_47403068del , CM000664.2:g.47403067_47403068del	GRCh38
NC_000002.11:g.47630206_47630207del , CM000664.1:g.47630206_47630207del	GRCh37
NC_000002.10:g.47483710_47483711del	NCBI36
NG_007110.2:g.4944_4945del , LRG_218:g.4944_4945del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543555.6:c.-139_-138del	ENSP00000442697.1:n.-139_-138del
ENST00000233146.6:c.-125_-124del	ENSP00000233146.2:n.-125_-124del
ENST00000454849.5:c.-139_-138del	ENSP00000411482.1:n.-139_-138del
ENST00000543555.5:c.-139_-138del	ENSP00000442697.1:n.-139_-138del
NM_000251.2:c.-125_-124del , LRG_218t1:c.-125_-124del	NP_000242.1:n.-125_-124del
NM_001258281.1:c.-139_-138del	NP_001245210.1:n.-139_-138del