Canonical Allele Identifier: CA1087449803

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113901670
• gnomAD v3: 6-31269317-TTCAG-T
• gnomAD v4: 6-31269317-TTCAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269318_31269321del , CM000668.2:g.31269318_31269321del	GRCh38
NC_000006.11:g.31237095_31237098del , CM000668.1:g.31237095_31237098del	GRCh37
NC_000006.10:g.31345074_31345077del	NCBI36
NG_029422.2:g.7811_7814del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1096+17_1096+20del MANE Select	ENSP00000365402.5:n.1096+17_1096+20del
ENST00000376228.9:c.1096+17_1096+20del	ENSP00000365402.5:n.1096+17_1096+20del
ENST00000376237.8:c.*683+17_*683+20del	ENSP00000365412.4:n.*683+17_*683+20del
ENST00000383329.7:c.1114+17_1114+20del	ENSP00000372819.3:n.1114+17_1114+20del
ENST00000466892.5:n.329+17_329+20del
ENST00000470363.5:n.854+17_854+20del
ENST00000487245.5:n.1455+17_1455+20del
NM_002117.5:c.1096+17_1096+20del	NP_002108.4:n.1096+17_1096+20del
NM_002117.6:c.1096+17_1096+20del MANE Select	NP_002108.4:n.1096+17_1096+20del