Canonical Allele Identifier: CA1612347153

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627491_15627492delinsAG , CM000668.2:g.15627491_15627492delinsAG	GRCh38
NC_000006.11:g.15627722_15627723delinsAG , CM000668.1:g.15627722_15627723delinsAG	GRCh37
NC_000006.10:g.15735701_15735702delinsAG	NCBI36
NG_009309.1:g.40549_40550delinsCT , LRG_588:g.40549_40550delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.223-17_223-16delinsCT MANE Select	ENSP00000341680.6:n.223-17_223-16delinsCT
ENST00000338950.9:c.223-17_223-16delinsCT	ENSP00000344718.5:n.223-17_223-16delinsCT
ENST00000344537.9:c.223-17_223-16delinsCT	ENSP00000341680.5:n.223-17_223-16delinsCT
ENST00000355917.7:c.172-17_172-16delinsCT	ENSP00000348183.4:n.172-17_172-16delinsCT
ENST00000506844.1:c.*221-17_*221-16delinsCT	ENSP00000424202.1:n.*221-17_*221-16delinsCT
ENST00000510395.5:c.*133-17_*133-16delinsCT	ENSP00000424685.1:n.*133-17_*133-16delinsCT
ENST00000511762.2:c.118-17_118-16delinsCT	ENSP00000427473.2:n.118-17_118-16delinsCT
ENST00000513680.5:c.*221-17_*221-16delinsCT	ENSP00000424357.1:n.*221-17_*221-16delinsCT
ENST00000515875.5:c.172-17_172-16delinsCT	ENSP00000425495.1:n.172-17_172-16delinsCT
ENST00000622898.4:c.118-17_118-16delinsCT	ENSP00000481997.1:n.118-17_118-16delinsCT
NM_001271667.1:c.-21-17_-21-16delinsCT	NP_001258596.1:n.-21-17_-21-16delinsCT
NM_001271668.1:c.172-17_172-16delinsCT	NP_001258597.1:n.172-17_172-16delinsCT
NM_001271669.1:c.118-17_118-16delinsCT	NP_001258598.1:n.118-17_118-16delinsCT
NM_032122.4:c.223-17_223-16delinsCT , LRG_588t1:c.223-17_223-16delinsCT	NP_115498.2:n.223-17_223-16delinsCT
NM_183040.2:c.223-17_223-16delinsCT , LRG_588t2:c.223-17_223-16delinsCT	NP_898861.1:n.223-17_223-16delinsCT
NR_036448.1:n.551-17_551-16delinsCT
XM_005249447.3:c.184-17_184-16delinsCT	XP_005249504.1:n.184-17_184-16delinsCT
XM_011514936.1:c.133-17_133-16delinsCT	XP_011513238.1:n.133-17_133-16delinsCT
XM_005249447.4:c.184-17_184-16delinsCT	XP_005249504.1:n.184-17_184-16delinsCT
XM_011514936.3:c.133-17_133-16delinsCT	XP_011513238.1:n.133-17_133-16delinsCT
NM_032122.5:c.223-17_223-16delinsCT MANE Select	NP_115498.2:n.223-17_223-16delinsCT
NR_036448.2:n.521-17_521-16delinsCT
NM_001271667.2:c.-21-17_-21-16delinsCT	NP_001258596.1:n.-21-17_-21-16delinsCT
NM_001271668.2:c.172-17_172-16delinsCT	NP_001258597.1:n.172-17_172-16delinsCT
NM_001271669.2:c.118-17_118-16delinsCT	NP_001258598.1:n.118-17_118-16delinsCT
NR_036448.3:n.521-17_521-16delinsCT