Canonical Allele Identifier: CA2677951261
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271144_31271145dup , CM000668.2:g.31271144_31271145dup GRCh38
NC_000006.11:g.31238921_31238922dup , CM000668.1:g.31238921_31238922dup GRCh37
NC_000006.10:g.31346900_31346901dup NCBI36
NG_029422.2:g.5987_5988dup

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.547_548dup MANE Select ENSP00000365402.5:p.Leu184ThrfsTer?
ENST00000376228.9:c.547_548dup ENSP00000365402.5:p.Leu184ThrfsTer?
ENST00000376237.8:c.*134_*135dup ENSP00000365412.4:n.*134_*135dup
ENST00000383329.7:c.547_548dup ENSP00000372819.3:p.Leu184ThrfsTer?
ENST00000415537.1:c.545_546dup
ENST00000484378.1:n.816_817dup
ENST00000487245.5:n.906_907dup
ENST00000495835.1:n.736_737dup
NM_002117.5:c.547_548dup NP_002108.4:p.Leu184ThrfsTer?
NM_002117.6:c.547_548dup MANE Select NP_002108.4:p.Leu184ThrfsTer?