Canonical Allele Identifier: CA1619080732
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271612G= , CM000668.2:g.31271612G= GRCh38
NC_000006.11:g.31239389G= , CM000668.1:g.31239389G= GRCh37
NC_000006.10:g.31347368G= NCBI36
NG_029422.2:g.5520C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.330C= MANE Select ENSP00000365402.5:p.Asn110=
ENST00000376228.9:c.330C= ENSP00000365402.5:p.Asn110=
ENST00000376237.8:c.330C= ENSP00000365412.4:p.Asn110=
ENST00000383329.7:c.330C= ENSP00000372819.3:p.Asn110=
ENST00000415537.1:c.328C=
ENST00000484378.1:n.349C=
ENST00000487245.5:n.439C=
ENST00000495835.1:n.519C=
NM_002117.5:c.330C= NP_002108.4:p.Asn110=
NM_002117.6:c.330C= MANE Select NP_002108.4:p.Asn110=