Canonical Allele Identifier: CA566286019

Gene: HLA-A

Linked Data

• dbSNP Id: rs1562681896
• gnomAD v2: 6-29910476-C-CCCGGGAAGCCGCG
• MyVariant Identifiers: chr6:g.29910476_29910477insCCGGGAAGCCGCG (hg19) ; chr6:g.29942699_29942700insCCGGGAAGCCGCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942700_29942701insCGGGAAGCCGCGC , CM000668.2:g.29942700_29942701insCGGGAAGCCGCGC	GRCh38
NC_000006.11:g.29910477_29910478insCGGGAAGCCGCGC , CM000668.1:g.29910477_29910478insCGGGAAGCCGCGC	GRCh37
NC_000006.10:g.30018456_30018457insCGGGAAGCCGCGC	NCBI36
NG_029217.2:g.5235_5236insCGGGAAGCCGCGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000492789.2:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000706892.1:n.350-57_350-56insCGGGAAGCCGCGC
ENST00000706893.1:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000516609.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000706894.1:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000516610.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000706895.1:n.350-57_350-56insCGGGAAGCCGCGC
ENST00000706896.1:n.350-57_350-56insCGGGAAGCCGCGC
ENST00000706897.1:n.350-57_350-56insCGGGAAGCCGCGC
ENST00000706898.1:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000516611.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000706899.1:n.350-57_350-56insCGGGAAGCCGCGC
ENST00000706901.1:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000516612.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000706902.1:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000516613.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000706903.1:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000516614.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000706904.1:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000516615.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000706905.1:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000516616.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000376809.10:c.74-57_74-56insCGGGAAGCCGCGC MANE Select	ENSP00000366005.5:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000638375.1:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000492789.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000376802.2:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000365998.2:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000376806.9:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000366002.5:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000376809.9:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000366005.5:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000396634.5:c.74-57_74-56insCGGGAAGCCGCGC	ENSP00000379873.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000429656.1:n.368_369insCGCGGCTTCCCGG
ENST00000461903.1:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000479320.5:n.74-57_74-56insCGGGAAGCCGCGC
ENST00000495183.5:n.76-57_76-56insCGGGAAGCCGCGC
ENST00000496081.5:n.80-57_80-56insCGGGAAGCCGCGC
NM_002116.7:c.74-57_74-56insCGGGAAGCCGCGC	NP_002107.3:n.74-57_74-56insCGGGAAGCCGCGC
NM_002116.8:c.74-57_74-56insCGGGAAGCCGCGC MANE Select	NP_002107.3:n.74-57_74-56insCGGGAAGCCGCGC