Canonical Allele Identifier: CA2677950952

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113907810
• gnomAD v4: 6-31270711-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270712_31270713del , CM000668.2:g.31270712_31270713del	GRCh38
NC_000006.11:g.31238489_31238490del , CM000668.1:g.31238489_31238490del	GRCh37
NC_000006.10:g.31346468_31346469del	NCBI36
NG_029422.2:g.6419_6420del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.620-228_620-227del MANE Select	ENSP00000365402.5:n.620-228_620-227del
ENST00000376228.9:c.620-228_620-227del	ENSP00000365402.5:n.620-228_620-227del
ENST00000376237.8:c.*207-228_*207-227del	ENSP00000365412.4:n.*207-228_*207-227del
ENST00000383329.7:c.620-228_620-227del	ENSP00000372819.3:n.620-228_620-227del
ENST00000415537.1:c.618-228_618-227del
ENST00000487245.5:n.979-228_979-227del
ENST00000495835.1:n.809-228_809-227del
NM_002117.5:c.620-228_620-227del	NP_002108.4:n.620-228_620-227del
NM_002117.6:c.620-228_620-227del MANE Select	NP_002108.4:n.620-228_620-227del