Canonical Allele Identifier: CA2695198653

Gene: MSH3

Linked Data

• ClinVar Variation Id: 2673492
• ClinVar RCV Id: RCV003459061

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675129_80675133del , CM000667.2:g.80675129_80675133del	GRCh38
NC_000005.9:g.79970948_79970952del , CM000667.1:g.79970948_79970952del	GRCh37
NC_000005.8:g.80006704_80006708del	NCBI36
NG_016607.1:g.25655_25659del
NG_016607.2:g.25655_25659del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+1_1173+5del
ENST00000658259.1:c.1005+1_1005+5del
ENST00000667069.1:c.1173+1_1173+5del
ENST00000670357.1:c.1173+1_1173+5del
ENST00000265081.6:c.1173+1_1173+5del
NM_002439.4:c.1173+1_1173+5del
NM_002439.5:c.1173+1_1173+5del