Canonical Allele Identifier: CA136024253
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs199474600
MyVariant Identifiers: chr6:g.29911476del (hg19) chr6:g.29943699del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943699del , CM000668.2:g.29943699del GRCh38
NC_000006.11:g.29911476del , CM000668.1:g.29911476del GRCh37
NC_000006.10:g.30019455del NCBI36
NG_029217.2:g.6235del

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.619+156del ENSP00000492789.2:n.619+156del
ENST00000706892.1:n.1051del
ENST00000706893.1:c.619+156del ENSP00000516609.1:n.619+156del
ENST00000706894.1:c.619+156del ENSP00000516610.1:n.619+156del
ENST00000706895.1:n.895+156del
ENST00000706896.1:n.1051del
ENST00000706897.1:n.895+156del
ENST00000706898.1:c.619+156del ENSP00000516611.1:n.619+156del
ENST00000706899.1:n.1051del
ENST00000706900.1:c.535+156del ENSP00000516617.1:n.535+156del
ENST00000706901.1:c.619+156del ENSP00000516612.1:n.619+156del
ENST00000706902.1:c.619+156del ENSP00000516613.1:n.619+156del
ENST00000706903.1:c.619+156del ENSP00000516614.1:n.619+156del
ENST00000706904.1:c.619+156del ENSP00000516615.1:n.619+156del
ENST00000706905.1:c.619+156del ENSP00000516616.1:n.619+156del
ENST00000376809.10:c.619+156del MANE Select ENSP00000366005.5:n.619+156del
ENST00000638375.1:c.619+156del ENSP00000492789.1:n.619+156del
ENST00000376802.2:c.619+156del ENSP00000365998.2:n.619+156del
ENST00000376806.9:c.619+156del ENSP00000366002.5:n.619+156del
ENST00000376809.9:c.619+156del ENSP00000366005.5:n.619+156del
ENST00000396634.5:c.619+156del ENSP00000379873.1:n.619+156del
ENST00000461903.1:n.860+156del
ENST00000479320.5:n.860+156del
ENST00000495183.5:n.862+156del
ENST00000496081.5:n.436+156del
NM_002116.7:c.619+156del NP_002107.3:n.619+156del
NM_002116.8:c.619+156del MANE Select NP_002107.3:n.619+156del
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