Canonical Allele Identifier: CA2573333215
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.[29942881C>T;29943451A>T;29943462T>C;29943463T>A] , CM000668.2:g.[29942881C>T;29943451A>T;29943462T>C;29943463T>A] GRCh38
NC_000006.11:g.[29910658C>T;29911228A>T;29911239T>C;29911240T>A] , CM000668.1:g.[29910658C>T;29911228A>T;29911239T>C;29911240T>A] GRCh37
NC_000006.10:g.[30018637C>T;30019207A>T;30019218T>C;30019219T>A] NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000492789.2:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000706892.1:n.[474C>T;803A>T;814T>C;815T>A]
ENST00000706893.1:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000516609.1:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000706894.1:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000516610.1:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000706895.1:n.[474C>T;803A>T;814T>C;815T>A]
ENST00000706896.1:n.[474C>T;803A>T;814T>C;815T>A]
ENST00000706897.1:n.[474C>T;803A>T;814T>C;815T>A]
ENST00000706898.1:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000516611.1:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000706899.1:n.[474C>T;803A>T;814T>C;815T>A]
ENST00000706900.1:c.[114C>T;443A>T;454T>C;455T>A] ENSP00000516617.1:p.[Ser38=;Glu148Val;Leu152Gln]
ENST00000706901.1:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000516612.1:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000706902.1:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000516613.1:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000706903.1:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000516614.1:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000706904.1:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000516615.1:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000706905.1:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000516616.1:p.[Ser66=;Glu176Val;Leu180Gln]
ENST00000376809.10:c.[198C>T;527A>T;538T>C;539T>A] MANE Select ENSP00000366005.5:p.[Ser66=;Glu176Val;Leu180Gln]
ENST00000638375.1:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000492789.1:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000376802.2:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000365998.2:p.[Ser66=;Glu176Val;Leu180Gln]
ENST00000376806.9:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000366002.5:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000376809.9:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000366005.5:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
ENST00000396634.5:c.[198C>T;527A>T;538T>C;539T>A] ENSP00000379873.1:p.[Ser66=;Glu176Val;Leu180Gln]
ENST00000461903.1:n.[198C>T;768A>T;779T>C;780T>A]
ENST00000479320.5:n.[198C>T;768A>T;779T>C;780T>A]
ENST00000495183.5:n.[200C>T;770A>T;781T>C;782T>A]
ENST00000496081.5:n.[177+27C>T;344A>T;355T>C;356T>A]
NM_002116.7:c.[198C>T;527A>T;538T>C;539T>A] NP_002107.3:p.[Ser66=;Glu176Val;Leu180=;Leu180Ter]
NM_002116.8:c.[198C>T;527A>T;538T>C;539T>A] MANE Select NP_002107.3:p.[Ser66=;Glu176Val;Leu180Gln]