Canonical Allele Identifier: CA823863635

Gene: HLA-C

Linked Data

• dbSNP Id: rs1281302584
• gnomAD v3: 6-31271493-GATCCAC-G
• gnomAD v4: 6-31271493-GATCCAC-G
• MyVariant Identifiers: chr6:g.31239271_31239276del (hg19) ; chr6:g.31271494_31271499del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271494_31271499del , CM000668.2:g.31271494_31271499del	GRCh38
NC_000006.11:g.31239271_31239276del , CM000668.1:g.31239271_31239276del	GRCh37
NC_000006.10:g.31347250_31347255del	NCBI36
NG_029422.2:g.5633_5638del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.343+100_343+105del MANE Select	ENSP00000365402.5:n.343+100_343+105del
ENST00000376228.9:c.343+100_343+105del	ENSP00000365402.5:n.343+100_343+105del
ENST00000376237.8:c.343+100_343+105del	ENSP00000365412.4:n.343+100_343+105del
ENST00000383329.7:c.343+100_343+105del	ENSP00000372819.3:n.343+100_343+105del
ENST00000415537.1:c.341+100_341+105del
ENST00000484378.1:n.462_467del
ENST00000487245.5:n.552_557del
ENST00000495835.1:n.532+100_532+105del
NM_002117.5:c.343+100_343+105del	NP_002108.4:n.343+100_343+105del
NM_002117.6:c.343+100_343+105del MANE Select	NP_002108.4:n.343+100_343+105del