Canonical Allele Identifier: CA2677951683
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271593_31271594del , CM000668.2:g.31271593_31271594del GRCh38
NC_000006.11:g.31239370_31239371del , CM000668.1:g.31239370_31239371del GRCh37
NC_000006.10:g.31347349_31347350del NCBI36
NG_029422.2:g.5539_5540del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+6_343+7del MANE Select ENSP00000365402.5:n.343+6_343+7del
ENST00000376228.9:c.343+6_343+7del ENSP00000365402.5:n.343+6_343+7del
ENST00000376237.8:c.343+6_343+7del ENSP00000365412.4:n.343+6_343+7del
ENST00000383329.7:c.343+6_343+7del ENSP00000372819.3:n.343+6_343+7del
ENST00000415537.1:c.341+6_341+7del
ENST00000484378.1:n.368_369del
ENST00000487245.5:n.458_459del
ENST00000495835.1:n.532+6_532+7del
NM_002117.5:c.343+6_343+7del NP_002108.4:n.343+6_343+7del
NM_002117.6:c.343+6_343+7del MANE Select NP_002108.4:n.343+6_343+7del