Canonical Allele Identifier: CA1619080583

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761338516

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271385_31271386insTCCGC , CM000668.2:g.31271385_31271386insTCCGC	GRCh38
NC_000006.11:g.31239162_31239163insTCCGC , CM000668.1:g.31239162_31239163insTCCGC	GRCh37
NC_000006.10:g.31347141_31347142insTCCGC	NCBI36
NG_029422.2:g.5748_5749insGGAGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.344-36_344-35insGGAGC MANE Select	ENSP00000365402.5:n.344-36_344-35insGGAGC
ENST00000376228.9:c.344-36_344-35insGGAGC	ENSP00000365402.5:n.344-36_344-35insGGAGC
ENST00000376237.8:c.344-53_344-52insGGAGC	ENSP00000365412.4:n.344-53_344-52insGGAGC
ENST00000383329.7:c.344-36_344-35insGGAGC	ENSP00000372819.3:n.344-36_344-35insGGAGC
ENST00000415537.1:c.342-36_342-35insGGAGC
ENST00000484378.1:n.577_578insGGAGC
ENST00000487245.5:n.667_668insGGAGC
ENST00000495835.1:n.533-36_533-35insGGAGC
NM_002117.5:c.344-36_344-35insGGAGC	NP_002108.4:n.344-36_344-35insGGAGC
NM_002117.6:c.344-36_344-35insGGAGC MANE Select	NP_002108.4:n.344-36_344-35insGGAGC