Canonical Allele Identifier: CA566688990

Gene: HLA-C

Linked Data

• dbSNP Id: rs1252707015
• gnomAD v2: 6-31239148-C-CCCCGT
• gnomAD v4: 6-31271371-C-CCCCGT
• MyVariant Identifiers: chr6:g.31239148_31239149insCCCGT (hg19) ; chr6:g.31271371_31271372insCCCGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271373_31271374insCGTCC , CM000668.2:g.31271373_31271374insCGTCC	GRCh38
NC_000006.11:g.31239150_31239151insCGTCC , CM000668.1:g.31239150_31239151insCGTCC	GRCh37
NC_000006.10:g.31347129_31347130insCGTCC	NCBI36
NG_029422.2:g.5760_5761insACGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.344-24_344-23insACGGG MANE Select	ENSP00000365402.5:n.344-24_344-23insACGGG...
ENST00000376228.9:c.344-24_344-23insACGGG	ENSP00000365402.5:n.344-24_344-23insACGGG...
ENST00000376237.8:c.344-41_344-40insACGGG	ENSP00000365412.4:n.344-41_344-40insACGGG...
ENST00000383329.7:c.344-24_344-23insACGGG	ENSP00000372819.3:n.344-24_344-23insACGGG...
ENST00000415537.1:c.342-24_342-23insACGGG
ENST00000484378.1:n.589_590insACGGG
ENST00000487245.5:n.679_680insACGGG
ENST00000495835.1:n.533-24_533-23insACGGG
NM_002117.5:c.344-24_344-23insACGGG	NP_002108.4:n.344-24_344-23insACGGG
NM_002117.6:c.344-24_344-23insACGGG MANE Select	NP_002108.4:n.344-24_344-23insACGGG