Canonical Allele Identifier: CA362869633

Gene: DTNBP1

Linked Data

• MyVariant Identifiers: chr6:g.15638030T>A (hg19) ; chr6:g.15637799T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15637799T>A , CM000668.2:g.15637799T>A	GRCh38
NC_000006.11:g.15638030T>A , CM000668.1:g.15638030T>A	GRCh37
NC_000006.10:g.15746009T>A	NCBI36
NG_009309.1:g.30242A>T , LRG_588:g.30242A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344537.10:c.167A>T MANE Select	ENSP00000341680.6:p.Glu56Val
ENST00000338950.9:c.167A>T	ENSP00000344718.5:p.Glu56Val
ENST00000344537.9:c.167A>T	ENSP00000341680.5:p.Glu56Val
ENST00000355917.7:c.116A>T	ENSP00000348183.4:p.Glu39Val
ENST00000506844.1:c.*165A>T	ENSP00000424202.1:n.*165A>T
ENST00000510395.5:c.*77A>T	ENSP00000424685.1:n.*77A>T
ENST00000511762.2:c.62A>T	ENSP00000427473.2:p.Glu21Val
ENST00000513680.5:c.*165A>T	ENSP00000424357.1:n.*165A>T
ENST00000515875.5:c.116A>T	ENSP00000425495.1:p.Glu39Val
ENST00000622898.4:c.62A>T	ENSP00000481997.1:p.Glu21Val
NM_001271667.1:c.-77A>T	NP_001258596.1:n.-77A>T
NM_001271668.1:c.116A>T	NP_001258597.1:p.Glu39Val
NM_001271669.1:c.62A>T	NP_001258598.1:p.Glu21Val
NM_032122.4:c.167A>T , LRG_588t1:c.167A>T	NP_115498.2:p.Glu56Val
NM_183040.2:c.167A>T , LRG_588t2:c.167A>T	NP_898861.1:p.Glu56Val
NR_036448.1:n.495A>T
XM_005249447.3:c.128A>T	XP_005249504.1:p.Glu43Val
XM_011514936.1:c.77A>T	XP_011513238.1:p.Glu26Val
XM_005249447.4:c.128A>T	XP_005249504.1:p.Glu43Val
XM_011514936.3:c.77A>T	XP_011513238.1:p.Glu26Val
NM_032122.5:c.167A>T MANE Select	NP_115498.2:p.Glu56Val
NR_036448.2:n.465A>T
NM_001271667.2:c.-77A>T	NP_001258596.1:n.-77A>T
NM_001271668.2:c.116A>T	NP_001258597.1:p.Glu39Val
NM_001271669.2:c.62A>T	NP_001258598.1:p.Glu21Val
NR_036448.3:n.465A>T