Canonical Allele Identifier: CA1612354195

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15633257_15633261delinsATTGT , CM000668.2:g.15633257_15633261delinsATTGT	GRCh38
NC_000006.11:g.15633488_15633492delinsATTGT , CM000668.1:g.15633488_15633492delinsATTGT	GRCh37
NC_000006.10:g.15741467_15741471delinsATTGT	NCBI36
NG_009309.1:g.34780_34784delinsACAAT , LRG_588:g.34780_34784delinsACAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.222+4483_222+4487delinsACAAT MANE Select	ENSP00000341680.6:n.222+4483_222+4487delinsACAAT
ENST00000338950.9:c.222+4483_222+4487delinsACAAT	ENSP00000344718.5:n.222+4483_222+4487delinsACAAT
ENST00000344537.9:c.222+4483_222+4487delinsACAAT	ENSP00000341680.5:n.222+4483_222+4487delinsACAAT
ENST00000355917.7:c.171+4483_171+4487delinsACAAT	ENSP00000348183.4:n.171+4483_171+4487delinsACAAT
ENST00000506844.1:c.*220+4483_*220+4487delinsACAAT	ENSP00000424202.1:n.*220+4483_*220+4487delinsACAAT
ENST00000510395.5:c.*132+4483_*132+4487delinsACAAT	ENSP00000424685.1:n.*132+4483_*132+4487delinsACAAT
ENST00000511762.2:c.117+4483_117+4487delinsACAAT	ENSP00000427473.2:n.117+4483_117+4487delinsACAAT
ENST00000513680.5:c.*220+4483_*220+4487delinsACAAT	ENSP00000424357.1:n.*220+4483_*220+4487delinsACAAT
ENST00000515875.5:c.171+4483_171+4487delinsACAAT	ENSP00000425495.1:n.171+4483_171+4487delinsACAAT
ENST00000622898.4:c.117+4483_117+4487delinsACAAT	ENSP00000481997.1:n.117+4483_117+4487delinsACAAT
NM_001271667.1:c.-22+4483_-22+4487delinsACAAT	NP_001258596.1:n.-22+4483_-22+4487delinsACAAT
NM_001271668.1:c.171+4483_171+4487delinsACAAT	NP_001258597.1:n.171+4483_171+4487delinsACAAT
NM_001271669.1:c.117+4483_117+4487delinsACAAT	NP_001258598.1:n.117+4483_117+4487delinsACAAT
NM_032122.4:c.222+4483_222+4487delinsACAAT , LRG_588t1:c.222+4483_222+4487delinsACAAT	NP_115498.2:n.222+4483_222+4487delinsACAAT
NM_183040.2:c.222+4483_222+4487delinsACAAT , LRG_588t2:c.222+4483_222+4487delinsACAAT	NP_898861.1:n.222+4483_222+4487delinsACAAT
NR_036448.1:n.550+4483_550+4487delinsACAAT
XM_005249447.3:c.183+4483_183+4487delinsACAAT	XP_005249504.1:n.183+4483_183+4487delinsACAAT
XM_011514936.1:c.132+4483_132+4487delinsACAAT	XP_011513238.1:n.132+4483_132+4487delinsACAAT
XM_005249447.4:c.183+4483_183+4487delinsACAAT	XP_005249504.1:n.183+4483_183+4487delinsACAAT
XM_011514936.3:c.132+4483_132+4487delinsACAAT	XP_011513238.1:n.132+4483_132+4487delinsACAAT
NM_032122.5:c.222+4483_222+4487delinsACAAT MANE Select	NP_115498.2:n.222+4483_222+4487delinsACAAT
NR_036448.2:n.520+4483_520+4487delinsACAAT
NM_001271667.2:c.-22+4483_-22+4487delinsACAAT	NP_001258596.1:n.-22+4483_-22+4487delinsACAAT
NM_001271668.2:c.171+4483_171+4487delinsACAAT	NP_001258597.1:n.171+4483_171+4487delinsACAAT
NM_001271669.2:c.117+4483_117+4487delinsACAAT	NP_001258598.1:n.117+4483_117+4487delinsACAAT
NR_036448.3:n.520+4483_520+4487delinsACAAT