Canonical Allele Identifier: CA566688985

Gene: HLA-C

Linked Data

• dbSNP Id: rs1440714024
• gnomAD v2: 6-31238973-T-TCCC
• MyVariant Identifiers: chr6:g.31238973_31238974insCCC (hg19) ; chr6:g.31271196_31271197insCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271197_31271198insCCC , CM000668.2:g.31271197_31271198insCCC	GRCh38
NC_000006.11:g.31238974_31238975insCCC , CM000668.1:g.31238974_31238975insCCC	GRCh37
NC_000006.10:g.31346953_31346954insCCC	NCBI36
NG_029422.2:g.5935_5936insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.495_496insGGG MANE Select	ENSP00000365402.5:p.Gln165_Ile166insGly
ENST00000376228.9:c.495_496insGGG	ENSP00000365402.5:p.Gln165_Ile166insGly
ENST00000376237.8:c.*82_*83insGGG	ENSP00000365412.4:n.*82_*83insGGG
ENST00000383329.7:c.495_496insGGG	ENSP00000372819.3:p.Gln165_Ile166insGly
ENST00000415537.1:c.493_494insGGG
ENST00000484378.1:n.764_765insGGG
ENST00000487245.5:n.854_855insGGG
ENST00000495835.1:n.684_685insGGG
NM_002117.5:c.495_496insGGG	NP_002108.4:p.Gln165_Ile166insGly
NM_002117.6:c.495_496insGGG MANE Select	NP_002108.4:p.Gln165_Ile166insGly