Canonical Allele Identifier: CA1612354131

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15633202G= , CM000668.2:g.15633202G=	GRCh38
NC_000006.11:g.15633433G= , CM000668.1:g.15633433G=	GRCh37
NC_000006.10:g.15741412G=	NCBI36
NG_009309.1:g.34839C= , LRG_588:g.34839C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000344537.10:c.222+4542C= MANE Select	ENSP00000341680.6:n.222+4542C=
ENST00000338950.9:c.222+4542C=	ENSP00000344718.5:n.222+4542C=
ENST00000344537.9:c.222+4542C=	ENSP00000341680.5:n.222+4542C=
ENST00000355917.7:c.171+4542C=	ENSP00000348183.4:n.171+4542C=
ENST00000506844.1:c.*220+4542C=	ENSP00000424202.1:n.*220+4542C=
ENST00000510395.5:c.*132+4542C=	ENSP00000424685.1:n.*132+4542C=
ENST00000511762.2:c.117+4542C=	ENSP00000427473.2:n.117+4542C=
ENST00000513680.5:c.*220+4542C=	ENSP00000424357.1:n.*220+4542C=
ENST00000515875.5:c.171+4542C=	ENSP00000425495.1:n.171+4542C=
ENST00000622898.4:c.117+4542C=	ENSP00000481997.1:n.117+4542C=
NM_001271667.1:c.-22+4542C=	NP_001258596.1:n.-22+4542C=
NM_001271668.1:c.171+4542C=	NP_001258597.1:n.171+4542C=
NM_001271669.1:c.117+4542C=	NP_001258598.1:n.117+4542C=
NM_032122.4:c.222+4542C= , LRG_588t1:c.222+4542C=	NP_115498.2:n.222+4542C=
NM_183040.2:c.222+4542C= , LRG_588t2:c.222+4542C=	NP_898861.1:n.222+4542C=
NR_036448.1:n.550+4542C=
XM_005249447.3:c.183+4542C=	XP_005249504.1:n.183+4542C=
XM_011514936.1:c.132+4542C=	XP_011513238.1:n.132+4542C=
XM_005249447.4:c.183+4542C=	XP_005249504.1:n.183+4542C=
XM_011514936.3:c.132+4542C=	XP_011513238.1:n.132+4542C=
NM_032122.5:c.222+4542C= MANE Select	NP_115498.2:n.222+4542C=
NR_036448.2:n.520+4542C=
NM_001271667.2:c.-22+4542C=	NP_001258596.1:n.-22+4542C=
NM_001271668.2:c.171+4542C=	NP_001258597.1:n.171+4542C=
NM_001271669.2:c.117+4542C=	NP_001258598.1:n.117+4542C=
NR_036448.3:n.520+4542C=