Canonical Allele Identifier: CA1612387917

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15650849_15650850delinsAC , CM000668.2:g.15650849_15650850delinsAC	GRCh38
NC_000006.11:g.15651080_15651081delinsAC , CM000668.1:g.15651080_15651081delinsAC	GRCh37
NC_000006.10:g.15759059_15759060delinsAC	NCBI36
NG_009309.1:g.17191_17192delinsGT , LRG_588:g.17191_17192delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000344537.10:c.161+463_161+464delinsGT MANE Select	ENSP00000341680.6:n.161+463_161+464delins...
ENST00000338950.9:c.161+463_161+464delinsGT	ENSP00000344718.5:n.161+463_161+464delins...
ENST00000344537.9:c.161+463_161+464delinsGT	ENSP00000341680.5:n.161+463_161+464delins...
ENST00000355917.7:c.110+1237_110+1238delinsGT	ENSP00000348183.4:n.110+1237_110+1238deli...
ENST00000506844.1:c.*159+463_*159+464delinsGT	ENSP00000424202.1:n.*159+463_*159+464deli...
ENST00000510395.5:c.*71+463_*71+464delinsGT	ENSP00000424685.1:n.*71+463_*71+464delins...
ENST00000511762.2:c.56+11964_56+11965delinsGT	ENSP00000427473.2:n.56+11964_56+11965deli...
ENST00000513680.5:c.*159+463_*159+464delinsGT	ENSP00000424357.1:n.*159+463_*159+464deli...
ENST00000515875.5:c.110+1237_110+1238delinsGT	ENSP00000425495.1:n.110+1237_110+1238deli...
ENST00000622898.4:c.56+11964_56+11965delinsGT	ENSP00000481997.1:n.56+11964_56+11965deli...
NM_001271667.1:c.-83+463_-83+464delinsGT	NP_001258596.1:n.-83+463_-83+464delinsGT
NM_001271668.1:c.110+1237_110+1238delinsGT	NP_001258597.1:n.110+1237_110+1238delinsG...
NM_001271669.1:c.56+11964_56+11965delinsGT	NP_001258598.1:n.56+11964_56+11965delinsG...
NM_032122.4:c.161+463_161+464delinsGT , LRG_588t1:c.161+463_161+464delinsGT	NP_115498.2:n.161+463_161+464delinsGT
NM_183040.2:c.161+463_161+464delinsGT , LRG_588t2:c.161+463_161+464delinsGT	NP_898861.1:n.161+463_161+464delinsGT
NR_036448.1:n.489+463_489+464delinsGT
XM_005249447.3:c.122+463_122+464delinsGT	XP_005249504.1:n.122+463_122+464delinsGT
XM_011514936.1:c.71+1237_71+1238delinsGT	XP_011513238.1:n.71+1237_71+1238delinsGT
XM_005249447.4:c.122+463_122+464delinsGT	XP_005249504.1:n.122+463_122+464delinsGT
XM_011514936.3:c.71+1237_71+1238delinsGT	XP_011513238.1:n.71+1237_71+1238delinsGT
NM_032122.5:c.161+463_161+464delinsGT MANE Select	NP_115498.2:n.161+463_161+464delinsGT
NR_036448.2:n.459+463_459+464delinsGT
NM_001271667.2:c.-83+463_-83+464delinsGT	NP_001258596.1:n.-83+463_-83+464delinsGT
NM_001271668.2:c.110+1237_110+1238delinsGT	NP_001258597.1:n.110+1237_110+1238delinsG...
NM_001271669.2:c.56+11964_56+11965delinsGT	NP_001258598.1:n.56+11964_56+11965delinsG...
NR_036448.3:n.459+463_459+464delinsGT