Canonical Allele Identifier: CA2677950301
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270001-A-ATCC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270001_31270002insTCC , CM000668.2:g.31270001_31270002insTCC GRCh38
NC_000006.11:g.31237778_31237779insTCC , CM000668.1:g.31237778_31237779insTCC GRCh37
NC_000006.10:g.31345757_31345758insTCC NCBI36
NG_029422.2:g.7130_7131insGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.979_980insGGA MANE Select ENSP00000365402.5:p.Val327delinsGlyMet
ENST00000376228.9:c.979_980insGGA ENSP00000365402.5:p.Val327delinsGlyMet
ENST00000376237.8:c.*566_*567insGGA ENSP00000365412.4:n.*566_*567insGGA
ENST00000383329.7:c.979_980insGGA ENSP00000372819.3:p.Val327delinsGlyMet
ENST00000470363.5:n.297_298insGGA
ENST00000487245.5:n.1338_1339insGGA
NM_002117.5:c.979_980insGGA NP_002108.4:p.Val327delinsGlyMet
NM_002117.6:c.979_980insGGA MANE Select NP_002108.4:p.Val327delinsGlyMet
Search 100 bp 5'
Search 100 bp 3'