Canonical Allele Identifier: CA1558493810

Gene: MSH3

Linked Data

• dbSNP Id: rs1749813112

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675160_80675166del , CM000667.2:g.80675160_80675166del	GRCh38
NC_000005.9:g.79970979_79970985del , CM000667.1:g.79970979_79970985del	GRCh37
NC_000005.8:g.80006735_80006741del	NCBI36
NG_016607.1:g.25686_25692del
NG_016607.2:g.25686_25692del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+32_1173+38del MANE Select	ENSP00000265081.6:n.1173+32_1173+38del
ENST00000658259.1:c.1005+32_1005+38del	ENSP00000499617.1:n.1005+32_1005+38del
ENST00000667069.1:c.1173+32_1173+38del	ENSP00000499502.1:n.1173+32_1173+38del
ENST00000670357.1:c.1173+32_1173+38del	ENSP00000499791.1:n.1173+32_1173+38del
ENST00000265081.6:c.1173+32_1173+38del	ENSP00000265081.6:n.1173+32_1173+38del
NM_002439.4:c.1173+32_1173+38del	NP_002430.3:n.1173+32_1173+38del
NM_002439.5:c.1173+32_1173+38del MANE Select	NP_002430.3:n.1173+32_1173+38del