Canonical Allele Identifier: CA1612387916

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15650844_15650846delinsGAC , CM000668.2:g.15650844_15650846delinsGAC	GRCh38
NC_000006.11:g.15651075_15651077delinsGAC , CM000668.1:g.15651075_15651077delinsGAC	GRCh37
NC_000006.10:g.15759054_15759056delinsGAC	NCBI36
NG_009309.1:g.17195_17197delinsGTC , LRG_588:g.17195_17197delinsGTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000344537.10:c.161+467_161+469delinsGTC MANE Select	ENSP00000341680.6:n.161+467_161+469delins...
ENST00000338950.9:c.161+467_161+469delinsGTC	ENSP00000344718.5:n.161+467_161+469delins...
ENST00000344537.9:c.161+467_161+469delinsGTC	ENSP00000341680.5:n.161+467_161+469delins...
ENST00000355917.7:c.110+1241_110+1243delinsGTC	ENSP00000348183.4:n.110+1241_110+1243deli...
ENST00000506844.1:c.*159+467_*159+469delinsGTC	ENSP00000424202.1:n.*159+467_*159+469deli...
ENST00000510395.5:c.*71+467_*71+469delinsGTC	ENSP00000424685.1:n.*71+467_*71+469delins...
ENST00000511762.2:c.56+11968_56+11970delinsGTC	ENSP00000427473.2:n.56+11968_56+11970deli...
ENST00000513680.5:c.*159+467_*159+469delinsGTC	ENSP00000424357.1:n.*159+467_*159+469deli...
ENST00000515875.5:c.110+1241_110+1243delinsGTC	ENSP00000425495.1:n.110+1241_110+1243deli...
ENST00000622898.4:c.56+11968_56+11970delinsGTC	ENSP00000481997.1:n.56+11968_56+11970deli...
NM_001271667.1:c.-83+467_-83+469delinsGTC	NP_001258596.1:n.-83+467_-83+469delinsGTC...
NM_001271668.1:c.110+1241_110+1243delinsGTC	NP_001258597.1:n.110+1241_110+1243delinsG...
NM_001271669.1:c.56+11968_56+11970delinsGTC	NP_001258598.1:n.56+11968_56+11970delinsG...
NM_032122.4:c.161+467_161+469delinsGTC , LRG_588t1:c.161+467_161+469delinsGTC	NP_115498.2:n.161+467_161+469delinsGTC
NM_183040.2:c.161+467_161+469delinsGTC , LRG_588t2:c.161+467_161+469delinsGTC	NP_898861.1:n.161+467_161+469delinsGTC
NR_036448.1:n.489+467_489+469delinsGTC
XM_005249447.3:c.122+467_122+469delinsGTC	XP_005249504.1:n.122+467_122+469delinsGTC...
XM_011514936.1:c.71+1241_71+1243delinsGTC	XP_011513238.1:n.71+1241_71+1243delinsGTC...
XM_005249447.4:c.122+467_122+469delinsGTC	XP_005249504.1:n.122+467_122+469delinsGTC...
XM_011514936.3:c.71+1241_71+1243delinsGTC	XP_011513238.1:n.71+1241_71+1243delinsGTC...
NM_032122.5:c.161+467_161+469delinsGTC MANE Select	NP_115498.2:n.161+467_161+469delinsGTC
NR_036448.2:n.459+467_459+469delinsGTC
NM_001271667.2:c.-83+467_-83+469delinsGTC	NP_001258596.1:n.-83+467_-83+469delinsGTC...
NM_001271668.2:c.110+1241_110+1243delinsGTC	NP_001258597.1:n.110+1241_110+1243delinsG...
NM_001271669.2:c.56+11968_56+11970delinsGTC	NP_001258598.1:n.56+11968_56+11970delinsG...
NR_036448.3:n.459+467_459+469delinsGTC