Canonical Allele Identifier: CA2677950254

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269944-CCGCTCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269946_31269952del , CM000668.2:g.31269946_31269952del	GRCh38
NC_000006.11:g.31237723_31237729del , CM000668.1:g.31237723_31237729del	GRCh37
NC_000006.10:g.31345702_31345708del	NCBI36
NG_029422.2:g.7181_7187del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+15_1015+21del MANE Select	ENSP00000365402.5:n.1015+15_1015+21del
ENST00000376228.9:c.1015+15_1015+21del	ENSP00000365402.5:n.1015+15_1015+21del
ENST00000376237.8:c.*602+15_*602+21del	ENSP00000365412.4:n.*602+15_*602+21del
ENST00000383329.7:c.1015+15_1015+21del	ENSP00000372819.3:n.1015+15_1015+21del
ENST00000470363.5:n.348_354del
ENST00000487245.5:n.1374+15_1374+21del
NM_002117.5:c.1015+15_1015+21del	NP_002108.4:n.1015+15_1015+21del
NM_002117.6:c.1015+15_1015+21del MANE Select	NP_002108.4:n.1015+15_1015+21del