Canonical Allele Identifier: CA1612384594

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627369T= , CM000668.2:g.15627369T=	GRCh38
NC_000006.11:g.15627600T= , CM000668.1:g.15627600T=	GRCh37
NC_000006.10:g.15735579T=	NCBI36
NG_009309.1:g.40672A= , LRG_588:g.40672A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.329A= MANE Select	ENSP00000341680.6:p.Asp110=
ENST00000338950.9:c.329A=	ENSP00000344718.5:p.Asp110=
ENST00000344537.9:c.329A=	ENSP00000341680.5:p.Asp110=
ENST00000355917.7:c.278A=	ENSP00000348183.4:p.Asp93=
ENST00000506844.1:c.*327A=	ENSP00000424202.1:n.*327A=
ENST00000510395.5:c.*239A=	ENSP00000424685.1:n.*239A=
ENST00000511762.2:c.224A=	ENSP00000427473.2:p.Asp75=
ENST00000513680.5:c.*327A=	ENSP00000424357.1:n.*327A=
ENST00000515875.5:c.278A=	ENSP00000425495.1:p.Asp93=
ENST00000622898.4:c.224A=	ENSP00000481997.1:p.Asp75=
NM_001271667.1:c.86A=	NP_001258596.1:p.Asp29=
NM_001271668.1:c.278A=	NP_001258597.1:p.Asp93=
NM_001271669.1:c.224A=	NP_001258598.1:p.Asp75=
NM_032122.4:c.329A= , LRG_588t1:c.329A=	NP_115498.2:p.Asp110=
NM_183040.2:c.329A= , LRG_588t2:c.329A=	NP_898861.1:p.Asp110=
NR_036448.1:n.657A=
XM_005249447.3:c.290A=	XP_005249504.1:p.Asp97=
XM_011514936.1:c.239A=	XP_011513238.1:p.Asp80=
XM_005249447.4:c.290A=	XP_005249504.1:p.Asp97=
XM_011514936.3:c.239A=	XP_011513238.1:p.Asp80=
NM_032122.5:c.329A= MANE Select	NP_115498.2:p.Asp110=
NR_036448.2:n.627A=
NM_001271667.2:c.86A=	NP_001258596.1:p.Asp29=
NM_001271668.2:c.278A=	NP_001258597.1:p.Asp93=
NM_001271669.2:c.224A=	NP_001258598.1:p.Asp75=
NR_036448.3:n.627A=