Canonical Allele Identifier: CA2767180117

Gene: MSH3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675275_80675276del , CM000667.2:g.80675275_80675276del	GRCh38
NC_000005.9:g.79971094_79971095del , CM000667.1:g.79971094_79971095del	GRCh37
NC_000005.8:g.80006850_80006851del	NCBI36
NG_016607.1:g.25801_25802del
NG_016607.2:g.25801_25802del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+147_1173+148del MANE Select	ENSP00000265081.6:n.1173+147_1173+148del
ENST00000658259.1:c.1005+147_1005+148del	ENSP00000499617.1:n.1005+147_1005+148del
ENST00000667069.1:c.1173+147_1173+148del	ENSP00000499502.1:n.1173+147_1173+148del
ENST00000670357.1:c.1173+147_1173+148del	ENSP00000499791.1:n.1173+147_1173+148del
ENST00000265081.6:c.1173+147_1173+148del	ENSP00000265081.6:n.1173+147_1173+148del
NM_002439.4:c.1173+147_1173+148del	NP_002430.3:n.1173+147_1173+148del
NM_002439.5:c.1173+147_1173+148del MANE Select	NP_002430.3:n.1173+147_1173+148del