Canonical Allele Identifier: CA1619080522
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271326C= , CM000668.2:g.31271326C= GRCh38
NC_000006.11:g.31239103C= , CM000668.1:g.31239103C= GRCh37
NC_000006.10:g.31347082C= NCBI36
NG_029422.2:g.5806G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.366G= MANE Select ENSP00000365402.5:p.Met122=
ENST00000376228.9:c.366G= ENSP00000365402.5:p.Met122=
ENST00000376237.8:c.349G= ENSP00000365412.4:p.Val117=
ENST00000383329.7:c.366G= ENSP00000372819.3:p.Met122=
ENST00000415537.1:c.364G=
ENST00000484378.1:n.635G=
ENST00000487245.5:n.725G=
ENST00000495835.1:n.555G=
NM_002117.5:c.366G= NP_002108.4:p.Met122=
NM_002117.6:c.366G= MANE Select NP_002108.4:p.Met122=