Canonical Allele Identifier: CA1612384608

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627403C= , CM000668.2:g.15627403C=	GRCh38
NC_000006.11:g.15627634C= , CM000668.1:g.15627634C=	GRCh37
NC_000006.10:g.15735613C=	NCBI36
NG_009309.1:g.40638G= , LRG_588:g.40638G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.295G= MANE Select	ENSP00000341680.6:p.Glu99=
ENST00000338950.9:c.295G=	ENSP00000344718.5:p.Glu99=
ENST00000344537.9:c.295G=	ENSP00000341680.5:p.Glu99=
ENST00000355917.7:c.244G=	ENSP00000348183.4:p.Glu82=
ENST00000506844.1:c.*293G=	ENSP00000424202.1:n.*293G=
ENST00000510395.5:c.*205G=	ENSP00000424685.1:n.*205G=
ENST00000511762.2:c.190G=	ENSP00000427473.2:p.Glu64=
ENST00000513680.5:c.*293G=	ENSP00000424357.1:n.*293G=
ENST00000515875.5:c.244G=	ENSP00000425495.1:p.Glu82=
ENST00000622898.4:c.190G=	ENSP00000481997.1:p.Glu64=
NM_001271667.1:c.52G=	NP_001258596.1:p.Glu18=
NM_001271668.1:c.244G=	NP_001258597.1:p.Glu82=
NM_001271669.1:c.190G=	NP_001258598.1:p.Glu64=
NM_032122.4:c.295G= , LRG_588t1:c.295G=	NP_115498.2:p.Glu99=
NM_183040.2:c.295G= , LRG_588t2:c.295G=	NP_898861.1:p.Glu99=
NR_036448.1:n.623G=
XM_005249447.3:c.256G=	XP_005249504.1:p.Glu86=
XM_011514936.1:c.205G=	XP_011513238.1:p.Glu69=
XM_005249447.4:c.256G=	XP_005249504.1:p.Glu86=
XM_011514936.3:c.205G=	XP_011513238.1:p.Glu69=
NM_032122.5:c.295G= MANE Select	NP_115498.2:p.Glu99=
NR_036448.2:n.593G=
NM_001271667.2:c.52G=	NP_001258596.1:p.Glu18=
NM_001271668.2:c.244G=	NP_001258597.1:p.Glu82=
NM_001271669.2:c.190G=	NP_001258598.1:p.Glu64=
NR_036448.3:n.593G=