Canonical Allele Identifier: CA2677949802

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269530-G-GGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269531_31269532insCTG , CM000668.2:g.31269531_31269532insCTG	GRCh38
NC_000006.11:g.31237308_31237309insCTG , CM000668.1:g.31237308_31237309insCTG	GRCh37
NC_000006.10:g.31345287_31345288insCTG	NCBI36
NG_029422.2:g.7601_7602insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1016-6_1016-5insAGC MANE Select	ENSP00000365402.5:n.1016-6_1016-5insAGC
ENST00000376228.9:c.1016-6_1016-5insAGC	ENSP00000365402.5:n.1016-6_1016-5insAGC
ENST00000376237.8:c.*603-6_*603-5insAGC	ENSP00000365412.4:n.*603-6_*603-5insAGC
ENST00000383329.7:c.1028_1029insAGC	ENSP00000372819.3:p.Pro343_Thr344insAla
ENST00000466892.5:n.136_137insAGC
ENST00000470363.5:n.768_769insAGC
ENST00000487245.5:n.1375-6_1375-5insAGC
NM_002117.5:c.1016-6_1016-5insAGC	NP_002108.4:n.1016-6_1016-5insAGC
NM_002117.6:c.1016-6_1016-5insAGC MANE Select	NP_002108.4:n.1016-6_1016-5insAGC