Canonical Allele Identifier: CA2677951305

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271208-T-TCCAAGAGCGCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271208_31271209insCCAAGAGCGCAG , CM000668.2:g.31271208_31271209insCCAAGAGCGCAG	GRCh38
NC_000006.11:g.31238985_31238986insCCAAGAGCGCAG , CM000668.1:g.31238985_31238986insCCAAGAGCGCAG	GRCh37
NC_000006.10:g.31346964_31346965insCCAAGAGCGCAG	NCBI36
NG_029422.2:g.5923_5924insCTGCGCTCTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.483_484insCTGCGCTCTTGG MANE Select	ENSP00000365402.5:p.Asp161_Thr162insLeuArgSerTrp
ENST00000376228.9:c.483_484insCTGCGCTCTTGG	ENSP00000365402.5:p.Asp161_Thr162insLeuArgSerTrp
ENST00000376237.8:c.*70_*71insCTGCGCTCTTGG	ENSP00000365412.4:n.*70_*71insCTGCGCTCTTGG
ENST00000383329.7:c.483_484insCTGCGCTCTTGG	ENSP00000372819.3:p.Asp161_Thr162insLeuArgSerTrp
ENST00000415537.1:c.481_482insCTGCGCTCTTGG
ENST00000484378.1:n.752_753insCTGCGCTCTTGG
ENST00000487245.5:n.842_843insCTGCGCTCTTGG
ENST00000495835.1:n.672_673insCTGCGCTCTTGG
NM_002117.5:c.483_484insCTGCGCTCTTGG	NP_002108.4:p.Asp161_Thr162insLeuArgSerTrp
NM_002117.6:c.483_484insCTGCGCTCTTGG MANE Select	NP_002108.4:p.Asp161_Thr162insLeuArgSerTrp