Canonical Allele Identifier: CA2709330049

Gene: MSH3

Linked Data

• dbSNP Id: rs2112816201

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675179_80675180insTCTCATC , CM000667.2:g.80675179_80675180insTCTCATC	GRCh38
NC_000005.9:g.79970998_79970999insTCTCATC , CM000667.1:g.79970998_79970999insTCTCATC	GRCh37
NC_000005.8:g.80006754_80006755insTCTCATC	NCBI36
NG_016607.1:g.25705_25706insTCTCATC
NG_016607.2:g.25705_25706insTCTCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+51_1173+52insTCTCATC MANE Select	ENSP00000265081.6:n.1173+51_1173+52insTCTCATC
ENST00000658259.1:c.1005+51_1005+52insTCTCATC	ENSP00000499617.1:n.1005+51_1005+52insTCTCATC
ENST00000667069.1:c.1173+51_1173+52insTCTCATC	ENSP00000499502.1:n.1173+51_1173+52insTCTCATC
ENST00000670357.1:c.1173+51_1173+52insTCTCATC	ENSP00000499791.1:n.1173+51_1173+52insTCTCATC
ENST00000265081.6:c.1173+51_1173+52insTCTCATC	ENSP00000265081.6:n.1173+51_1173+52insTCTCATC
NM_002439.4:c.1173+51_1173+52insTCTCATC	NP_002430.3:n.1173+51_1173+52insTCTCATC
NM_002439.5:c.1173+51_1173+52insTCTCATC MANE Select	NP_002430.3:n.1173+51_1173+52insTCTCATC