Canonical Allele Identifier: CA2677950912

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270669-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270670_31270671del , CM000668.2:g.31270670_31270671del	GRCh38
NC_000006.11:g.31238447_31238448del , CM000668.1:g.31238447_31238448del	GRCh37
NC_000006.10:g.31346426_31346427del	NCBI36
NG_029422.2:g.6461_6462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.620-186_620-185del MANE Select	ENSP00000365402.5:n.620-186_620-185del
ENST00000376228.9:c.620-186_620-185del	ENSP00000365402.5:n.620-186_620-185del
ENST00000376237.8:c.*207-186_*207-185del	ENSP00000365412.4:n.*207-186_*207-185del
ENST00000383329.7:c.620-186_620-185del	ENSP00000372819.3:n.620-186_620-185del
ENST00000415537.1:c.618-186_618-185del
ENST00000487245.5:n.979-186_979-185del
ENST00000495835.1:n.809-186_809-185del
NM_002117.5:c.620-186_620-185del	NP_002108.4:n.620-186_620-185del
NM_002117.6:c.620-186_620-185del MANE Select	NP_002108.4:n.620-186_620-185del