Canonical Allele Identifier: CA2677950047

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269750-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269751_31269752del , CM000668.2:g.31269751_31269752del	GRCh38
NC_000006.11:g.31237528_31237529del , CM000668.1:g.31237528_31237529del	GRCh37
NC_000006.10:g.31345507_31345508del	NCBI36
NG_029422.2:g.7380_7381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+214_1015+215del MANE Select	ENSP00000365402.5:n.1015+214_1015+215del
ENST00000376228.9:c.1015+214_1015+215del	ENSP00000365402.5:n.1015+214_1015+215del
ENST00000376237.8:c.*602+214_*602+215del	ENSP00000365412.4:n.*602+214_*602+215del
ENST00000383329.7:c.1016-209_1016-208del	ENSP00000372819.3:n.1016-209_1016-208del
ENST00000470363.5:n.547_548del
ENST00000487245.5:n.1374+214_1374+215del
NM_002117.5:c.1015+214_1015+215del	NP_002108.4:n.1015+214_1015+215del
NM_002117.6:c.1015+214_1015+215del MANE Select	NP_002108.4:n.1015+214_1015+215del