Canonical Allele Identifier: CA1612347532

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627750_15627752delinsCCT , CM000668.2:g.15627750_15627752delinsCCT	GRCh38
NC_000006.11:g.15627981_15627983delinsCCT , CM000668.1:g.15627981_15627983delinsCCT	GRCh37
NC_000006.10:g.15735960_15735962delinsCCT	NCBI36
NG_009309.1:g.40289_40291delinsAGG , LRG_588:g.40289_40291delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.223-277_223-275delinsAGG MANE Select	ENSP00000341680.6:n.223-277_223-275delinsAGG
ENST00000338950.9:c.223-277_223-275delinsAGG	ENSP00000344718.5:n.223-277_223-275delinsAGG
ENST00000344537.9:c.223-277_223-275delinsAGG	ENSP00000341680.5:n.223-277_223-275delinsAGG
ENST00000355917.7:c.172-277_172-275delinsAGG	ENSP00000348183.4:n.172-277_172-275delinsAGG
ENST00000506844.1:c.*221-277_*221-275delinsAGG	ENSP00000424202.1:n.*221-277_*221-275delinsAGG
ENST00000510395.5:c.*133-277_*133-275delinsAGG	ENSP00000424685.1:n.*133-277_*133-275delinsAGG
ENST00000511762.2:c.118-277_118-275delinsAGG	ENSP00000427473.2:n.118-277_118-275delinsAGG
ENST00000513680.5:c.*221-277_*221-275delinsAGG	ENSP00000424357.1:n.*221-277_*221-275delinsAGG
ENST00000515875.5:c.172-277_172-275delinsAGG	ENSP00000425495.1:n.172-277_172-275delinsAGG
ENST00000622898.4:c.118-277_118-275delinsAGG	ENSP00000481997.1:n.118-277_118-275delinsAGG
NM_001271667.1:c.-21-277_-21-275delinsAGG	NP_001258596.1:n.-21-277_-21-275delinsAGG
NM_001271668.1:c.172-277_172-275delinsAGG	NP_001258597.1:n.172-277_172-275delinsAGG
NM_001271669.1:c.118-277_118-275delinsAGG	NP_001258598.1:n.118-277_118-275delinsAGG
NM_032122.4:c.223-277_223-275delinsAGG , LRG_588t1:c.223-277_223-275delinsAGG	NP_115498.2:n.223-277_223-275delinsAGG
NM_183040.2:c.223-277_223-275delinsAGG , LRG_588t2:c.223-277_223-275delinsAGG	NP_898861.1:n.223-277_223-275delinsAGG
NR_036448.1:n.551-277_551-275delinsAGG
XM_005249447.3:c.184-277_184-275delinsAGG	XP_005249504.1:n.184-277_184-275delinsAGG
XM_011514936.1:c.133-277_133-275delinsAGG	XP_011513238.1:n.133-277_133-275delinsAGG
XM_005249447.4:c.184-277_184-275delinsAGG	XP_005249504.1:n.184-277_184-275delinsAGG
XM_011514936.3:c.133-277_133-275delinsAGG	XP_011513238.1:n.133-277_133-275delinsAGG
NM_032122.5:c.223-277_223-275delinsAGG MANE Select	NP_115498.2:n.223-277_223-275delinsAGG
NR_036448.2:n.521-277_521-275delinsAGG
NM_001271667.2:c.-21-277_-21-275delinsAGG	NP_001258596.1:n.-21-277_-21-275delinsAGG
NM_001271668.2:c.172-277_172-275delinsAGG	NP_001258597.1:n.172-277_172-275delinsAGG
NM_001271669.2:c.118-277_118-275delinsAGG	NP_001258598.1:n.118-277_118-275delinsAGG
NR_036448.3:n.521-277_521-275delinsAGG