Canonical Allele Identifier: CA1612384632

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627454T= , CM000668.2:g.15627454T=	GRCh38
NC_000006.11:g.15627685T= , CM000668.1:g.15627685T=	GRCh37
NC_000006.10:g.15735664T=	NCBI36
NG_009309.1:g.40587A= , LRG_588:g.40587A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.244A= MANE Select	ENSP00000341680.6:p.Met82=
ENST00000338950.9:c.244A=	ENSP00000344718.5:p.Met82=
ENST00000344537.9:c.244A=	ENSP00000341680.5:p.Met82=
ENST00000355917.7:c.193A=	ENSP00000348183.4:p.Met65=
ENST00000506844.1:c.*242A=	ENSP00000424202.1:n.*242A=
ENST00000510395.5:c.*154A=	ENSP00000424685.1:n.*154A=
ENST00000511762.2:c.139A=	ENSP00000427473.2:p.Met47=
ENST00000513680.5:c.*242A=	ENSP00000424357.1:n.*242A=
ENST00000515875.5:c.193A=	ENSP00000425495.1:p.Met65=
ENST00000622898.4:c.139A=	ENSP00000481997.1:p.Met47=
NM_001271667.1:c.1A=	NP_001258596.1:p.Met1=
NM_001271668.1:c.193A=	NP_001258597.1:p.Met65=
NM_001271669.1:c.139A=	NP_001258598.1:p.Met47=
NM_032122.4:c.244A= , LRG_588t1:c.244A=	NP_115498.2:p.Met82=
NM_183040.2:c.244A= , LRG_588t2:c.244A=	NP_898861.1:p.Met82=
NR_036448.1:n.572A=
XM_005249447.3:c.205A=	XP_005249504.1:p.Met69=
XM_011514936.1:c.154A=	XP_011513238.1:p.Met52=
XM_005249447.4:c.205A=	XP_005249504.1:p.Met69=
XM_011514936.3:c.154A=	XP_011513238.1:p.Met52=
NM_032122.5:c.244A= MANE Select	NP_115498.2:p.Met82=
NR_036448.2:n.542A=
NM_001271667.2:c.1A=	NP_001258596.1:p.Met1=
NM_001271668.2:c.193A=	NP_001258597.1:p.Met65=
NM_001271669.2:c.139A=	NP_001258598.1:p.Met47=
NR_036448.3:n.542A=