Canonical Allele Identifier: CA1619078667
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs745972874

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269987_31269988insAAC , CM000668.2:g.31269987_31269988insAAC GRCh38
NC_000006.11:g.31237764_31237765insAAC , CM000668.1:g.31237764_31237765insAAC GRCh37
NC_000006.10:g.31345743_31345744insAAC NCBI36
NG_029422.2:g.7144_7145insGTT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.993_994insGTT MANE Select ENSP00000365402.5:p.Met331_Met332insVal
ENST00000376228.9:c.993_994insGTT ENSP00000365402.5:p.Met331_Met332insVal
ENST00000376237.8:c.*580_*581insGTT ENSP00000365412.4:n.*580_*581insGTT
ENST00000383329.7:c.993_994insGTT ENSP00000372819.3:p.Met331_Met332insVal
ENST00000470363.5:n.311_312insGTT
ENST00000487245.5:n.1352_1353insGTT
NM_002117.5:c.993_994insGTT NP_002108.4:p.Met331_Met332insVal
NM_002117.6:c.993_994insGTT MANE Select NP_002108.4:p.Met331_Met332insVal