Canonical Allele Identifier: CA2677950942

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270704-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270706_31270707del , CM000668.2:g.31270706_31270707del	GRCh38
NC_000006.11:g.31238483_31238484del , CM000668.1:g.31238483_31238484del	GRCh37
NC_000006.10:g.31346462_31346463del	NCBI36
NG_029422.2:g.6426_6427del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.620-221_620-220del MANE Select	ENSP00000365402.5:n.620-221_620-220del
ENST00000376228.9:c.620-221_620-220del	ENSP00000365402.5:n.620-221_620-220del
ENST00000376237.8:c.*207-221_*207-220del	ENSP00000365412.4:n.*207-221_*207-220del
ENST00000383329.7:c.620-221_620-220del	ENSP00000372819.3:n.620-221_620-220del
ENST00000415537.1:c.618-221_618-220del
ENST00000487245.5:n.979-221_979-220del
ENST00000495835.1:n.809-221_809-220del
NM_002117.5:c.620-221_620-220del	NP_002108.4:n.620-221_620-220del
NM_002117.6:c.620-221_620-220del MANE Select	NP_002108.4:n.620-221_620-220del