Canonical Allele Identifier: CA2677949607

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269300-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269303_31269304del , CM000668.2:g.31269303_31269304del	GRCh38
NC_000006.11:g.31237080_31237081del , CM000668.1:g.31237080_31237081del	GRCh37
NC_000006.10:g.31345059_31345060del	NCBI36
NG_029422.2:g.7830_7831del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1096+36_1096+37del MANE Select	ENSP00000365402.5:n.1096+36_1096+37del
ENST00000376228.9:c.1096+36_1096+37del	ENSP00000365402.5:n.1096+36_1096+37del
ENST00000376237.8:c.*683+36_*683+37del	ENSP00000365412.4:n.*683+36_*683+37del
ENST00000383329.7:c.1114+36_1114+37del	ENSP00000372819.3:n.1114+36_1114+37del
ENST00000466892.5:n.329+36_329+37del
ENST00000470363.5:n.854+36_854+37del
ENST00000487245.5:n.1455+36_1455+37del
NM_002117.5:c.1096+36_1096+37del	NP_002108.4:n.1096+36_1096+37del
NM_002117.6:c.1096+36_1096+37del MANE Select	NP_002108.4:n.1096+36_1096+37del