Canonical Allele Identifier: CA1619674972

Gene: HLA-DQB1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659744_32659746delinsTCA , CM000668.2:g.32659744_32659746delinsTCA	GRCh38
NC_000006.11:g.32627521_32627523delinsTCA , CM000668.1:g.32627521_32627523delinsTCA	GRCh37
NC_000006.10:g.32735499_32735501delinsTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*490_*492delinsTGA MANE Select	ENSP00000407332.2:n.*490_*492delinsTGA
ENST00000374943.8:c.*490_*492delinsTGA	ENSP00000364080.4:n.*490_*492delinsTGA
ENST00000399079.7:c.*490_*492delinsTGA	ENSP00000382029.3:n.*490_*492delinsTGA
ENST00000399082.7:c.*490_*492delinsTGA	ENSP00000382032.3:n.*490_*492delinsTGA
ENST00000399084.5:c.*490_*492delinsTGA	ENSP00000382034.1:n.*490_*492delinsTGA
ENST00000434651.6:c.*490_*492delinsTGA	ENSP00000407332.2:n.*490_*492delinsTGA
ENST00000487676.1:n.4365_4367delinsTGA
NM_001243961.1:c.*490_*492delinsTGA	NP_001230890.1:n.*490_*492delinsTGA
NM_002123.4:c.*490_*492delinsTGA	NP_002114.3:n.*490_*492delinsTGA
NM_001243961.2:c.*490_*492delinsTGA	NP_001230890.1:n.*490_*492delinsTGA
NM_002123.5:c.*490_*492delinsTGA MANE Select	NP_002114.3:n.*490_*492delinsTGA