Canonical Allele Identifier: CA2709329933

Gene: MSH3

Linked Data

• dbSNP Id: rs2112816191

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675175_80675176insAG , CM000667.2:g.80675175_80675176insAG	GRCh38
NC_000005.9:g.79970994_79970995insAG , CM000667.1:g.79970994_79970995insAG	GRCh37
NC_000005.8:g.80006750_80006751insAG	NCBI36
NG_016607.1:g.25701_25702insAG
NG_016607.2:g.25701_25702insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+47_1173+48insAG MANE Select	ENSP00000265081.6:n.1173+47_1173+48insAG
ENST00000658259.1:c.1005+47_1005+48insAG	ENSP00000499617.1:n.1005+47_1005+48insAG
ENST00000667069.1:c.1173+47_1173+48insAG	ENSP00000499502.1:n.1173+47_1173+48insAG
ENST00000670357.1:c.1173+47_1173+48insAG	ENSP00000499791.1:n.1173+47_1173+48insAG
ENST00000265081.6:c.1173+47_1173+48insAG	ENSP00000265081.6:n.1173+47_1173+48insAG
NM_002439.4:c.1173+47_1173+48insAG	NP_002430.3:n.1173+47_1173+48insAG
NM_002439.5:c.1173+47_1173+48insAG MANE Select	NP_002430.3:n.1173+47_1173+48insAG