Canonical Allele Identifier: CA1619077401
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269176A= , CM000668.2:g.31269176A= GRCh38
NC_000006.11:g.31236953A= , CM000668.1:g.31236953A= GRCh37
NC_000006.10:g.31344932A= NCBI36
NG_029422.2:g.7956T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1097-3T= MANE Select ENSP00000365402.5:n.1097-3T=
ENST00000376228.9:c.1097-3T= ENSP00000365402.5:n.1097-3T=
ENST00000376237.8:c.*684-3T= ENSP00000365412.4:n.*684-3T=
ENST00000383329.7:c.1115-3T= ENSP00000372819.3:n.1115-3T=
ENST00000466892.5:n.330-3T=
ENST00000470363.5:n.855-3T=
ENST00000487245.5:n.1456-3T=
NM_002117.5:c.1097-3T= NP_002108.4:n.1097-3T=
NM_002117.6:c.1097-3T= MANE Select NP_002108.4:n.1097-3T=