Canonical Allele Identifier: CA566410002

Gene: HLA-DPA1

Linked Data

• dbSNP Id: rs1280153184
• gnomAD v2: 6-33037877-T-TA
• gnomAD v3: 6-33070100-T-TA
• gnomAD v4: 6-33070100-T-TA
• MyVariant Identifiers: chr6:g.33037877_33037878insA (hg19) ; chr6:g.33070100_33070101insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33070100_33070101insA , CM000668.2:g.33070100_33070101insA	GRCh38
NC_000006.11:g.33037877_33037878insA , CM000668.1:g.33037877_33037878insA	GRCh37
NC_000006.10:g.33145855_33145856insA	NCBI36
NG_033241.1:g.15678_15679insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692443.1:c.101-215_101-214insT MANE Select	ENSP00000509163.1:n.101-215_101-214insT
ENST00000419277.5:c.101-215_101-214insT	ENSP00000393566.1:n.101-215_101-214insT
ENST00000453337.1:c.101-215_101-214insT	ENSP00000390929.1:n.101-215_101-214insT
ENST00000463066.1:n.196-215_196-214insT
ENST00000476642.5:n.77-215_77-214insT
ENST00000479107.1:n.146-215_146-214insT
NM_001242524.1:c.101-215_101-214insT	NP_001229453.1:n.101-215_101-214insT
NM_001242525.1:c.101-215_101-214insT	NP_001229454.1:n.101-215_101-214insT
NM_033554.3:c.101-215_101-214insT	NP_291032.2:n.101-215_101-214insT
XM_011514559.1:c.101-215_101-214insT	XP_011512861.1:n.101-215_101-214insT
NM_001242524.2:c.101-215_101-214insT	NP_001229453.1:n.101-215_101-214insT
NM_001242525.2:c.101-215_101-214insT	NP_001229454.1:n.101-215_101-214insT