Canonical Allele Identifier: CA2678151065

Gene: HLA-DQB1

Linked Data

• gnomAD v4: 6-32659608-G-GTTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659608_32659609insTTTA , CM000668.2:g.32659608_32659609insTTTA	GRCh38
NC_000006.11:g.32627385_32627386insTTTA , CM000668.1:g.32627385_32627386insTTTA	GRCh37
NC_000006.10:g.32735363_32735364insTTTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*627_*628insTAAA MANE Select	ENSP00000407332.2:n.*627_*628insTAAA
ENST00000374943.8:c.*627_*628insTAAA	ENSP00000364080.4:n.*627_*628insTAAA
ENST00000399079.7:c.*627_*628insTAAA	ENSP00000382029.3:n.*627_*628insTAAA
ENST00000399082.7:c.*627_*628insTAAA	ENSP00000382032.3:n.*627_*628insTAAA
ENST00000399084.5:c.*627_*628insTAAA	ENSP00000382034.1:n.*627_*628insTAAA
ENST00000434651.6:c.*627_*628insTAAA	ENSP00000407332.2:n.*627_*628insTAAA
ENST00000487676.1:n.4502_4503insTAAA
NM_001243961.1:c.*627_*628insTAAA	NP_001230890.1:n.*627_*628insTAAA
NM_002123.4:c.*627_*628insTAAA	NP_002114.3:n.*627_*628insTAAA
NM_001243961.2:c.*627_*628insTAAA	NP_001230890.1:n.*627_*628insTAAA
NM_002123.5:c.*627_*628insTAAA MANE Select	NP_002114.3:n.*627_*628insTAAA