Canonical Allele Identifier: CA1612384627

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627439A= , CM000668.2:g.15627439A=	GRCh38
NC_000006.11:g.15627670A= , CM000668.1:g.15627670A=	GRCh37
NC_000006.10:g.15735649A=	NCBI36
NG_009309.1:g.40602T= , LRG_588:g.40602T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.259T= MANE Select	ENSP00000341680.6:p.Trp87=
ENST00000338950.9:c.259T=	ENSP00000344718.5:p.Trp87=
ENST00000344537.9:c.259T=	ENSP00000341680.5:p.Trp87=
ENST00000355917.7:c.208T=	ENSP00000348183.4:p.Trp70=
ENST00000506844.1:c.*257T=	ENSP00000424202.1:n.*257T=
ENST00000510395.5:c.*169T=	ENSP00000424685.1:n.*169T=
ENST00000511762.2:c.154T=	ENSP00000427473.2:p.Trp52=
ENST00000513680.5:c.*257T=	ENSP00000424357.1:n.*257T=
ENST00000515875.5:c.208T=	ENSP00000425495.1:p.Trp70=
ENST00000622898.4:c.154T=	ENSP00000481997.1:p.Trp52=
NM_001271667.1:c.16T=	NP_001258596.1:p.Trp6=
NM_001271668.1:c.208T=	NP_001258597.1:p.Trp70=
NM_001271669.1:c.154T=	NP_001258598.1:p.Trp52=
NM_032122.4:c.259T= , LRG_588t1:c.259T=	NP_115498.2:p.Trp87=
NM_183040.2:c.259T= , LRG_588t2:c.259T=	NP_898861.1:p.Trp87=
NR_036448.1:n.587T=
XM_005249447.3:c.220T=	XP_005249504.1:p.Trp74=
XM_011514936.1:c.169T=	XP_011513238.1:p.Trp57=
XM_005249447.4:c.220T=	XP_005249504.1:p.Trp74=
XM_011514936.3:c.169T=	XP_011513238.1:p.Trp57=
NM_032122.5:c.259T= MANE Select	NP_115498.2:p.Trp87=
NR_036448.2:n.557T=
NM_001271667.2:c.16T=	NP_001258596.1:p.Trp6=
NM_001271668.2:c.208T=	NP_001258597.1:p.Trp70=
NM_001271669.2:c.154T=	NP_001258598.1:p.Trp52=
NR_036448.3:n.557T=