Canonical Allele Identifier: CA2677950280
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269987_31269988dup , CM000668.2:g.31269987_31269988dup GRCh38
NC_000006.11:g.31237764_31237765dup , CM000668.1:g.31237764_31237765dup GRCh37
NC_000006.10:g.31345743_31345744dup NCBI36
NG_029422.2:g.7144_7145dup

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.993_994dup MANE Select ENSP00000365402.5:p.Met332ArgfsTer?
ENST00000376228.9:c.993_994dup ENSP00000365402.5:p.Met332ArgfsTer?
ENST00000376237.8:c.*580_*581dup ENSP00000365412.4:n.*580_*581dup
ENST00000383329.7:c.993_994dup ENSP00000372819.3:p.Met332ArgfsTer?
ENST00000470363.5:n.311_312dup
ENST00000487245.5:n.1352_1353dup
NM_002117.5:c.993_994dup NP_002108.4:p.Met332ArgfsTer?
NM_002117.6:c.993_994dup MANE Select NP_002108.4:p.Met332ArgfsTer?