Canonical Allele Identifier: CA1619080753
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271632T= , CM000668.2:g.31271632T= GRCh38
NC_000006.11:g.31239409T= , CM000668.1:g.31239409T= GRCh37
NC_000006.10:g.31347388T= NCBI36
NG_029422.2:g.5500A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.310A= MANE Select ENSP00000365402.5:p.Asn104=
ENST00000376228.9:c.310A= ENSP00000365402.5:p.Asn104=
ENST00000376237.8:c.310A= ENSP00000365412.4:p.Asn104=
ENST00000383329.7:c.310A= ENSP00000372819.3:p.Asn104=
ENST00000415537.1:c.308A=
ENST00000484378.1:n.329A=
ENST00000487245.5:n.419A=
ENST00000495835.1:n.499A=
NM_002117.5:c.310A= NP_002108.4:p.Asn104=
NM_002117.6:c.310A= MANE Select NP_002108.4:p.Asn104=