Canonical Allele Identifier: CA814453992

Gene: MSH3

Linked Data

• dbSNP Id: rs1300005622
• MyVariant Identifiers: chr5:g.79971012_79971013del (hg19) ; chr5:g.80675193_80675194del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675193_80675194del , CM000667.2:g.80675193_80675194del	GRCh38
NC_000005.9:g.79971012_79971013del , CM000667.1:g.79971012_79971013del	GRCh37
NC_000005.8:g.80006768_80006769del	NCBI36
NG_016607.1:g.25719_25720del
NG_016607.2:g.25719_25720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+65_1173+66del MANE Select	ENSP00000265081.6:n.1173+65_1173+66del
ENST00000658259.1:c.1005+65_1005+66del	ENSP00000499617.1:n.1005+65_1005+66del
ENST00000667069.1:c.1173+65_1173+66del	ENSP00000499502.1:n.1173+65_1173+66del
ENST00000670357.1:c.1173+65_1173+66del	ENSP00000499791.1:n.1173+65_1173+66del
ENST00000265081.6:c.1173+65_1173+66del	ENSP00000265081.6:n.1173+65_1173+66del
NM_002439.4:c.1173+65_1173+66del	NP_002430.3:n.1173+65_1173+66del
NM_002439.5:c.1173+65_1173+66del MANE Select	NP_002430.3:n.1173+65_1173+66del