Canonical Allele Identifier: CA2767180115

Gene: MSH3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675255_80675256del , CM000667.2:g.80675255_80675256del	GRCh38
NC_000005.9:g.79971074_79971075del , CM000667.1:g.79971074_79971075del	GRCh37
NC_000005.8:g.80006830_80006831del	NCBI36
NG_016607.1:g.25781_25782del
NG_016607.2:g.25781_25782del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+127_1173+128del MANE Select	ENSP00000265081.6:n.1173+127_1173+128del
ENST00000658259.1:c.1005+127_1005+128del	ENSP00000499617.1:n.1005+127_1005+128del
ENST00000667069.1:c.1173+127_1173+128del	ENSP00000499502.1:n.1173+127_1173+128del
ENST00000670357.1:c.1173+127_1173+128del	ENSP00000499791.1:n.1173+127_1173+128del
ENST00000265081.6:c.1173+127_1173+128del	ENSP00000265081.6:n.1173+127_1173+128del
NM_002439.4:c.1173+127_1173+128del	NP_002430.3:n.1173+127_1173+128del
NM_002439.5:c.1173+127_1173+128del MANE Select	NP_002430.3:n.1173+127_1173+128del