Canonical Allele Identifier: CA1619080661
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271502T= , CM000668.2:g.31271502T= GRCh38
NC_000006.11:g.31239279T= , CM000668.1:g.31239279T= GRCh37
NC_000006.10:g.31347258T= NCBI36
NG_029422.2:g.5630A=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+97A= MANE Select ENSP00000365402.5:n.343+97A=
ENST00000376228.9:c.343+97A= ENSP00000365402.5:n.343+97A=
ENST00000376237.8:c.343+97A= ENSP00000365412.4:n.343+97A=
ENST00000383329.7:c.343+97A= ENSP00000372819.3:n.343+97A=
ENST00000415537.1:c.341+97A=
ENST00000484378.1:n.459A=
ENST00000487245.5:n.549A=
ENST00000495835.1:n.532+97A=
NM_002117.5:c.343+97A= NP_002108.4:n.343+97A=
NM_002117.6:c.343+97A= MANE Select NP_002108.4:n.343+97A=