Canonical Allele Identifier: CA2600112703

Gene: MSH3

Linked Data

• ClinVar Variation Id: 2887303
• ClinVar RCV Id: RCV003722312
• gnomAD v3: 5-80674968-TTTAA-T
• gnomAD v4: 5-80674968-TTTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80674972_80674975del , CM000667.2:g.80674972_80674975del	GRCh38
NC_000005.9:g.79970791_79970794del , CM000667.1:g.79970791_79970794del	GRCh37
NC_000005.8:g.80006547_80006550del	NCBI36
NG_016607.1:g.25498_25501del
NG_016607.2:g.25498_25501del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1028-11_1028-8del MANE Select	ENSP00000265081.6:n.1028-11_1028-8del
ENST00000658259.1:c.860-11_860-8del	ENSP00000499617.1:n.860-11_860-8del
ENST00000667069.1:c.1028-11_1028-8del	ENSP00000499502.1:n.1028-11_1028-8del
ENST00000670357.1:c.1028-11_1028-8del	ENSP00000499791.1:n.1028-11_1028-8del
ENST00000265081.6:c.1028-11_1028-8del	ENSP00000265081.6:n.1028-11_1028-8del
NM_002439.4:c.1028-11_1028-8del	NP_002430.3:n.1028-11_1028-8del
NM_002439.5:c.1028-11_1028-8del MANE Select	NP_002430.3:n.1028-11_1028-8del