Canonical Allele Identifier: CA362869554

Gene: DTNBP1

Linked Data

• dbSNP Id: rs1760115169
• gnomAD v4: 6-15637763-T-C
• MyVariant Identifiers: chr6:g.15637994T>C (hg19) ; chr6:g.15637763T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15637763T>C , CM000668.2:g.15637763T>C	GRCh38
NC_000006.11:g.15637994T>C , CM000668.1:g.15637994T>C	GRCh37
NC_000006.10:g.15745973T>C	NCBI36
NG_009309.1:g.30278A>G , LRG_588:g.30278A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.203A>G MANE Select	ENSP00000341680.6:p.Asp68Gly
ENST00000338950.9:c.203A>G	ENSP00000344718.5:p.Asp68Gly
ENST00000344537.9:c.203A>G	ENSP00000341680.5:p.Asp68Gly
ENST00000355917.7:c.152A>G	ENSP00000348183.4:p.Asp51Gly
ENST00000506844.1:c.*201A>G	ENSP00000424202.1:n.*201A>G
ENST00000510395.5:c.*113A>G	ENSP00000424685.1:n.*113A>G
ENST00000511762.2:c.98A>G	ENSP00000427473.2:p.Asp33Gly
ENST00000513680.5:c.*201A>G	ENSP00000424357.1:n.*201A>G
ENST00000515875.5:c.152A>G	ENSP00000425495.1:p.Asp51Gly
ENST00000622898.4:c.98A>G	ENSP00000481997.1:p.Asp33Gly
NM_001271667.1:c.-41A>G	NP_001258596.1:n.-41A>G
NM_001271668.1:c.152A>G	NP_001258597.1:p.Asp51Gly
NM_001271669.1:c.98A>G	NP_001258598.1:p.Asp33Gly
NM_032122.4:c.203A>G , LRG_588t1:c.203A>G	NP_115498.2:p.Asp68Gly
NM_183040.2:c.203A>G , LRG_588t2:c.203A>G	NP_898861.1:p.Asp68Gly
NR_036448.1:n.531A>G
XM_005249447.3:c.164A>G	XP_005249504.1:p.Asp55Gly
XM_011514936.1:c.113A>G	XP_011513238.1:p.Asp38Gly
XM_005249447.4:c.164A>G	XP_005249504.1:p.Asp55Gly
XM_011514936.3:c.113A>G	XP_011513238.1:p.Asp38Gly
NM_032122.5:c.203A>G MANE Select	NP_115498.2:p.Asp68Gly
NR_036448.2:n.501A>G
NM_001271667.2:c.-41A>G	NP_001258596.1:n.-41A>G
NM_001271668.2:c.152A>G	NP_001258597.1:p.Asp51Gly
NM_001271669.2:c.98A>G	NP_001258598.1:p.Asp33Gly
NR_036448.3:n.501A>G