Canonical Allele Identifier: CA566285986

Gene: HLA-A

Linked Data

• gnomAD v2: 6-29912032-C-CAG
• gnomAD v4: 6-29944255-C-CAG
• MyVariant Identifiers: chr6:g.29912032_29912033insAG (hg19) ; chr6:g.29944255_29944256insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944256_29944257insGA , CM000668.2:g.29944256_29944257insGA	GRCh38
NC_000006.11:g.29912033_29912034insGA , CM000668.1:g.29912033_29912034insGA	GRCh37
NC_000006.10:g.30020012_30020013insGA	NCBI36
NG_029217.2:g.6792_6793insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.754_755insGA	ENSP00000492789.2:p.Thr252ArgfsTer?
ENST00000706892.1:n.1608_1609insGA
ENST00000706893.1:c.754_755insGA	ENSP00000516609.1:p.Thr252ArgfsTer?
ENST00000706894.1:c.754_755insGA	ENSP00000516610.1:p.Thr252ArgfsTer?
ENST00000706895.1:n.1030_1031insGA
ENST00000706896.1:n.1608_1609insGA
ENST00000706897.1:n.1030_1031insGA
ENST00000706898.1:c.754_755insGA	ENSP00000516611.1:p.Thr252ArgfsTer?
ENST00000706899.1:n.1608_1609insGA
ENST00000706900.1:c.670_671insGA	ENSP00000516617.1:p.Thr224ArgfsTer?
ENST00000706901.1:c.754_755insGA	ENSP00000516612.1:p.Thr252ArgfsTer?
ENST00000706902.1:c.754_755insGA	ENSP00000516613.1:p.Thr252ArgfsTer?
ENST00000706903.1:c.754_755insGA	ENSP00000516614.1:p.Thr252ArgfsTer?
ENST00000706904.1:c.754_755insGA	ENSP00000516615.1:p.Thr252ArgfsTer?
ENST00000706905.1:c.754_755insGA	ENSP00000516616.1:p.Thr252ArgfsTer?
ENST00000376809.10:c.754_755insGA MANE Select	ENSP00000366005.5:p.Thr252ArgfsTer?
ENST00000638375.1:c.754_755insGA	ENSP00000492789.1:p.Thr252ArgfsTer?
ENST00000376802.2:c.754_755insGA	ENSP00000365998.2:p.Thr252ArgfsTer?
ENST00000376806.9:c.754_755insGA	ENSP00000366002.5:p.Thr252ArgfsTer?
ENST00000376809.9:c.754_755insGA	ENSP00000366005.5:p.Thr252ArgfsTer?
ENST00000396634.5:c.754_755insGA	ENSP00000379873.1:p.Thr252ArgfsTer?
ENST00000461903.1:n.995_996insGA
ENST00000479320.5:n.995_996insGA
ENST00000495183.5:n.997_998insGA
ENST00000496081.5:n.571_572insGA
NM_002116.7:c.754_755insGA	NP_002107.3:p.Thr252ArgfsTer?
NM_002116.8:c.754_755insGA MANE Select	NP_002107.3:p.Thr252ArgfsTer?