Canonical Allele Identifier: CA449789921
Gene: HLA-C HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31237765del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269988del , CM000668.2:g.31269988del GRCh38
NC_000006.11:g.31237765del , CM000668.1:g.31237765del GRCh37
NC_000006.10:g.31345744del NCBI36
NG_029422.2:g.7144del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.993del MANE Select ENSP00000365402.5:p.Met331IlefsTer?
ENST00000376228.9:c.993del ENSP00000365402.5:p.Met331IlefsTer?
ENST00000376237.8:c.*580del ENSP00000365412.4:n.*580del
ENST00000383329.7:c.993del ENSP00000372819.3:p.Met331IlefsTer?
ENST00000470363.5:n.311del
ENST00000487245.5:n.1352del
NM_002117.5:c.993del NP_002108.4:p.Met331IlefsTer?
NM_002117.6:c.993del MANE Select NP_002108.4:p.Met331IlefsTer?