Canonical Allele Identifier: CA566689002

Gene: HLA-C

Linked Data

• gnomAD v2: 6-31239169-CCG-C
• gnomAD v4: 6-31271392-CCG-C
• MyVariant Identifiers: chr6:g.31239170_31239171del (hg19) ; chr6:g.31271393_31271394del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271394_31271395del , CM000668.2:g.31271394_31271395del	GRCh38
NC_000006.11:g.31239171_31239172del , CM000668.1:g.31239171_31239172del	GRCh37
NC_000006.10:g.31347150_31347151del	NCBI36
NG_029422.2:g.5738_5739del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.344-46_344-45del MANE Select	ENSP00000365402.5:n.344-46_344-45del
ENST00000376228.9:c.344-46_344-45del	ENSP00000365402.5:n.344-46_344-45del
ENST00000376237.8:c.344-63_344-62del	ENSP00000365412.4:n.344-63_344-62del
ENST00000383329.7:c.344-46_344-45del	ENSP00000372819.3:n.344-46_344-45del
ENST00000415537.1:c.342-46_342-45del
ENST00000484378.1:n.567_568del
ENST00000487245.5:n.657_658del
ENST00000495835.1:n.533-46_533-45del
NM_002117.5:c.344-46_344-45del	NP_002108.4:n.344-46_344-45del
NM_002117.6:c.344-46_344-45del MANE Select	NP_002108.4:n.344-46_344-45del