Canonical Allele Identifier: CA1619674979

Gene: HLA-DQB1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659746_32659749delinsACAC , CM000668.2:g.32659746_32659749delinsACAC	GRCh38
NC_000006.11:g.32627523_32627526delinsACAC , CM000668.1:g.32627523_32627526delinsACAC	GRCh37
NC_000006.10:g.32735501_32735504delinsACAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*487_*490delinsGTGT MANE Select	ENSP00000407332.2:n.*487_*490delinsGTGT
ENST00000374943.8:c.*487_*490delinsGTGT	ENSP00000364080.4:n.*487_*490delinsGTGT
ENST00000399079.7:c.*487_*490delinsGTGT	ENSP00000382029.3:n.*487_*490delinsGTGT
ENST00000399082.7:c.*487_*490delinsGTGT	ENSP00000382032.3:n.*487_*490delinsGTGT
ENST00000399084.5:c.*487_*490delinsGTGT	ENSP00000382034.1:n.*487_*490delinsGTGT
ENST00000434651.6:c.*487_*490delinsGTGT	ENSP00000407332.2:n.*487_*490delinsGTGT
ENST00000487676.1:n.4362_4365delinsGTGT
NM_001243961.1:c.*487_*490delinsGTGT	NP_001230890.1:n.*487_*490delinsGTGT
NM_002123.4:c.*487_*490delinsGTGT	NP_002114.3:n.*487_*490delinsGTGT
NM_001243961.2:c.*487_*490delinsGTGT	NP_001230890.1:n.*487_*490delinsGTGT
NM_002123.5:c.*487_*490delinsGTGT MANE Select	NP_002114.3:n.*487_*490delinsGTGT