Canonical Allele Identifier: CA2985887558

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271570_31271571del , CM000668.2:g.31271570_31271571del	GRCh38
NC_000006.11:g.31239347_31239348del , CM000668.1:g.31239347_31239348del	GRCh37
NC_000006.10:g.31347326_31347327del	NCBI36
NG_029422.2:g.5561_5562del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.343+28_343+29del MANE Select	ENSP00000365402.5:n.343+28_343+29del
ENST00000376228.9:c.343+28_343+29del	ENSP00000365402.5:n.343+28_343+29del
ENST00000376237.8:c.343+28_343+29del	ENSP00000365412.4:n.343+28_343+29del
ENST00000383329.7:c.343+28_343+29del	ENSP00000372819.3:n.343+28_343+29del
ENST00000415537.1:c.341+28_341+29del
ENST00000484378.1:n.390_391del
ENST00000487245.5:n.480_481del
ENST00000495835.1:n.532+28_532+29del
NM_002117.5:c.343+28_343+29del	NP_002108.4:n.343+28_343+29del
NM_002117.6:c.343+28_343+29del MANE Select	NP_002108.4:n.343+28_343+29del