Canonical Allele Identifier: CA136025112
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs199474644
MyVariant Identifiers: chr6:g.29912230del (hg19) chr6:g.29944453del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944453del , CM000668.2:g.29944453del GRCh38
NC_000006.11:g.29912230del , CM000668.1:g.29912230del GRCh37
NC_000006.10:g.30020209del NCBI36
NG_029217.2:g.6989del

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.895+56del ENSP00000492789.2:n.895+56del
ENST00000706892.1:n.1805del
ENST00000706893.1:c.896-13del ENSP00000516609.1:n.896-13del
ENST00000706894.1:c.896-47del ENSP00000516610.1:n.896-47del
ENST00000706895.1:n.1227del
ENST00000706896.1:n.1750-47del
ENST00000706897.1:n.1172-47del
ENST00000706898.1:c.896-47del ENSP00000516611.1:n.896-47del
ENST00000706899.1:n.1750-47del
ENST00000706900.1:c.812-47del ENSP00000516617.1:n.812-47del
ENST00000706901.1:c.896-47del ENSP00000516612.1:n.896-47del
ENST00000706902.1:c.896-47del ENSP00000516613.1:n.896-47del
ENST00000706903.1:c.896-47del ENSP00000516614.1:n.896-47del
ENST00000706904.1:c.896-47del ENSP00000516615.1:n.896-47del
ENST00000706905.1:c.896-47del ENSP00000516616.1:n.896-47del
ENST00000376809.10:c.896-47del MANE Select ENSP00000366005.5:n.896-47del
ENST00000638375.1:c.895+56del ENSP00000492789.1:n.895+56del
ENST00000376802.2:c.895+56del ENSP00000365998.2:n.895+56del
ENST00000376806.9:c.896-47del ENSP00000366002.5:n.896-47del
ENST00000376809.9:c.896-47del ENSP00000366005.5:n.896-47del
ENST00000396634.5:c.896-47del ENSP00000379873.1:n.896-47del
ENST00000461903.1:n.1137-47del
ENST00000479320.5:n.1137-47del
ENST00000495183.5:n.1139-47del
ENST00000496081.5:n.713-47del
NM_002116.7:c.896-47del NP_002107.3:n.896-47del
NM_002116.8:c.896-47del MANE Select NP_002107.3:n.896-47del
Search 100 bp 5'
Search 100 bp 3'