Canonical Allele Identifier: CA566689029

Gene: HLA-C

Linked Data

• gnomAD v2: 6-31239111-G-GGATGATGTGAGACCCTGGCCCCGGCCCCGCGGTCAGCCCCGTCCCCC
• MyVariant Identifiers: chr6:g.31239111_31239112insGATGATGTGAGACCCTGGCCCCGGCCCCGCGGTCAGCCCCGTCCCCC (hg19) ; chr6:g.31271334_31271335insGATGATGTGAGACCCTGGCCCCGGCCCCGCGGTCAGCCCCGTCCCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271336_31271337insTGATGTGAGACCCTGGCCCCGGCCCCGCGGTCAGCCCCGTCCCCCGA , CM000668.2:g.31271336_31271337insTGATGTGAGACCCTGGCCCCGGCCCCGCGGTCAGCCCCGTCCCCCGA	GRCh38
NC_000006.11:g.31239113_31239114insTGATGTGAGACCCTGGCCCCGGCCCCGCGGTCAGCCCCGTCCCCCGA , CM000668.1:g.31239113_31239114insTGATGTGAGACCCTGGCCCCGGCCCCGCGGTCAGCCCCGTCCCCCGA	GRCh37
NC_000006.10:g.31347092_31347093insTGATGTGAGACCCTGGCCCCGGCCCCGCGGTCAGCCCCGTCCCCCGA	NCBI36
NG_029422.2:g.5797_5798insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.357_358insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC MANE Select	ENSP00000365402.5:p.Gln120GlyfsTer5
ENST00000376228.9:c.357_358insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC	ENSP00000365402.5:p.Gln120GlyfsTer5
ENST00000376237.8:c.344-4_344-3insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC	ENSP00000365412.4:n.344-4_344-3insGGGGGAC...
ENST00000383329.7:c.357_358insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC	ENSP00000372819.3:p.Gln120GlyfsTer5
ENST00000415537.1:c.355_356insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC
ENST00000484378.1:n.626_627insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC
ENST00000487245.5:n.716_717insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC
ENST00000495835.1:n.546_547insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC
NM_002117.5:c.357_358insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC	NP_002108.4:p.Gln120GlyfsTer5
NM_002117.6:c.357_358insGGGGGACGGGGCTGACCGCGGGGCCGGGGCCAGGGTCTCACATCATC MANE Select	NP_002108.4:p.Gln120GlyfsTer5