Canonical Allele Identifier: CA2677951572
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271513_31271514del , CM000668.2:g.31271513_31271514del GRCh38
NC_000006.11:g.31239290_31239291del , CM000668.1:g.31239290_31239291del GRCh37
NC_000006.10:g.31347269_31347270del NCBI36
NG_029422.2:g.5620_5621del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+87_343+88del MANE Select ENSP00000365402.5:n.343+87_343+88del
ENST00000376228.9:c.343+87_343+88del ENSP00000365402.5:n.343+87_343+88del
ENST00000376237.8:c.343+87_343+88del ENSP00000365412.4:n.343+87_343+88del
ENST00000383329.7:c.343+87_343+88del ENSP00000372819.3:n.343+87_343+88del
ENST00000415537.1:c.341+87_341+88del
ENST00000484378.1:n.449_450del
ENST00000487245.5:n.539_540del
ENST00000495835.1:n.532+87_532+88del
NM_002117.5:c.343+87_343+88del NP_002108.4:n.343+87_343+88del
NM_002117.6:c.343+87_343+88del MANE Select NP_002108.4:n.343+87_343+88del