Canonical Allele Identifier: CA814453606

Gene: MSH3

Linked Data

• dbSNP Id: rs1223628381
• MyVariant Identifiers: chr5:g.79970732_79970734del (hg19) ; chr5:g.80674913_80674915del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80674917_80674919del , CM000667.2:g.80674917_80674919del	GRCh38
NC_000005.9:g.79970736_79970738del , CM000667.1:g.79970736_79970738del	GRCh37
NC_000005.8:g.80006492_80006494del	NCBI36
NG_016607.1:g.25443_25445del
NG_016607.2:g.25443_25445del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1028-66_1028-64del MANE Select	ENSP00000265081.6:n.1028-66_1028-64del
ENST00000658259.1:c.860-66_860-64del	ENSP00000499617.1:n.860-66_860-64del
ENST00000667069.1:c.1028-66_1028-64del	ENSP00000499502.1:n.1028-66_1028-64del
ENST00000670357.1:c.1028-66_1028-64del	ENSP00000499791.1:n.1028-66_1028-64del
ENST00000265081.6:c.1028-66_1028-64del	ENSP00000265081.6:n.1028-66_1028-64del
NM_002439.4:c.1028-66_1028-64del	NP_002430.3:n.1028-66_1028-64del
NM_002439.5:c.1028-66_1028-64del MANE Select	NP_002430.3:n.1028-66_1028-64del