Canonical Allele Identifier: CA2677951317
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271247_31271248del , CM000668.2:g.31271247_31271248del GRCh38
NC_000006.11:g.31239024_31239025del , CM000668.1:g.31239024_31239025del GRCh37
NC_000006.10:g.31347003_31347004del NCBI36
NG_029422.2:g.5885_5886del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.445_446del MANE Select ENSP00000365402.5:p.Ala149ProfsTer?
ENST00000376228.9:c.445_446del ENSP00000365402.5:p.Ala149ProfsTer?
ENST00000376237.8:c.*32_*33del ENSP00000365412.4:n.*32_*33del
ENST00000383329.7:c.445_446del ENSP00000372819.3:p.Ala149ProfsTer?
ENST00000415537.1:c.443_444del
ENST00000484378.1:n.714_715del
ENST00000487245.5:n.804_805del
ENST00000495835.1:n.634_635del
NM_002117.5:c.445_446del NP_002108.4:p.Ala149ProfsTer?
NM_002117.6:c.445_446del MANE Select NP_002108.4:p.Ala149ProfsTer?