Canonical Allele Identifier: CA1612384628

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627441T= , CM000668.2:g.15627441T=	GRCh38
NC_000006.11:g.15627672T= , CM000668.1:g.15627672T=	GRCh37
NC_000006.10:g.15735651T=	NCBI36
NG_009309.1:g.40600A= , LRG_588:g.40600A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.257A= MANE Select	ENSP00000341680.6:p.His86=
ENST00000338950.9:c.257A=	ENSP00000344718.5:p.His86=
ENST00000344537.9:c.257A=	ENSP00000341680.5:p.His86=
ENST00000355917.7:c.206A=	ENSP00000348183.4:p.His69=
ENST00000506844.1:c.*255A=	ENSP00000424202.1:n.*255A=
ENST00000510395.5:c.*167A=	ENSP00000424685.1:n.*167A=
ENST00000511762.2:c.152A=	ENSP00000427473.2:p.His51=
ENST00000513680.5:c.*255A=	ENSP00000424357.1:n.*255A=
ENST00000515875.5:c.206A=	ENSP00000425495.1:p.His69=
ENST00000622898.4:c.152A=	ENSP00000481997.1:p.His51=
NM_001271667.1:c.14A=	NP_001258596.1:p.His5=
NM_001271668.1:c.206A=	NP_001258597.1:p.His69=
NM_001271669.1:c.152A=	NP_001258598.1:p.His51=
NM_032122.4:c.257A= , LRG_588t1:c.257A=	NP_115498.2:p.His86=
NM_183040.2:c.257A= , LRG_588t2:c.257A=	NP_898861.1:p.His86=
NR_036448.1:n.585A=
XM_005249447.3:c.218A=	XP_005249504.1:p.His73=
XM_011514936.1:c.167A=	XP_011513238.1:p.His56=
XM_005249447.4:c.218A=	XP_005249504.1:p.His73=
XM_011514936.3:c.167A=	XP_011513238.1:p.His56=
NM_032122.5:c.257A= MANE Select	NP_115498.2:p.His86=
NR_036448.2:n.555A=
NM_001271667.2:c.14A=	NP_001258596.1:p.His5=
NM_001271668.2:c.206A=	NP_001258597.1:p.His69=
NM_001271669.2:c.152A=	NP_001258598.1:p.His51=
NR_036448.3:n.555A=