Canonical Allele Identifier: CA3643916

Gene: DTNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15524673C>T , CM000668.2:g.15524673C>T	GRCh38
NC_000006.11:g.15524904C>T , CM000668.1:g.15524904C>T	GRCh37
NC_000006.10:g.15632883C>T	NCBI36
NG_009309.1:g.143368G>A , LRG_588:g.143368G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.668-4G>A MANE Select	ENSP00000341680.6:n.668-4G>A
ENST00000338950.9:c.668-4G>A	ENSP00000344718.5:n.668-4G>A
ENST00000344537.9:c.668-4G>A	ENSP00000341680.5:n.668-4G>A
ENST00000355917.7:c.617-4G>A	ENSP00000348183.4:n.617-4G>A
ENST00000462989.6:c.200-4G>A	ENSP00000427239.1:n.200-4G>A
ENST00000506844.1:c.*666-4G>A	ENSP00000424202.1:n.*666-4G>A
ENST00000509674.1:c.119-4G>A	ENSP00000421797.1:n.119-4G>A
ENST00000510395.5:c.*578-4G>A	ENSP00000424685.1:n.*578-4G>A
ENST00000511762.2:c.563-4G>A	ENSP00000427473.2:n.563-4G>A
ENST00000513680.5:c.*670-6G>A	ENSP00000424357.1:n.*670-6G>A
ENST00000514651.1:n.309-4G>A
ENST00000515875.5:c.621-6G>A	ENSP00000425495.1:n.621-6G>A
ENST00000622898.4:c.563-4G>A	ENSP00000481997.1:n.563-4G>A
NM_001271667.1:c.425-4G>A	NP_001258596.1:n.425-4G>A
NM_001271668.1:c.617-4G>A	NP_001258597.1:n.617-4G>A
NM_001271669.1:c.563-4G>A	NP_001258598.1:n.563-4G>A
NM_032122.4:c.668-4G>A , LRG_588t1:c.668-4G>A	NP_115498.2:n.668-4G>A
NM_183040.2:c.668-4G>A , LRG_588t2:c.668-4G>A	NP_898861.1:n.668-4G>A
NR_036448.1:n.996-4G>A
XM_005249447.3:c.629-4G>A	XP_005249504.1:n.629-4G>A
XM_011514936.1:c.578-4G>A	XP_011513238.1:n.578-4G>A
XM_011514937.1:c.200-4G>A	XP_011513239.1:n.200-4G>A
XM_005249447.4:c.629-4G>A	XP_005249504.1:n.629-4G>A
XM_011514936.3:c.578-4G>A	XP_011513238.1:n.578-4G>A
XM_011514937.2:c.200-4G>A	XP_011513239.1:n.200-4G>A
XM_017011348.1:c.218-4G>A	XP_016866837.1:n.218-4G>A
XM_017011349.1:c.215-4G>A	XP_016866838.1:n.215-4G>A
XM_024446567.1:c.269-4G>A	XP_024302335.1:n.269-4G>A
NM_032122.5:c.668-4G>A MANE Select	NP_115498.2:n.668-4G>A
NR_036448.2:n.966-4G>A
NM_001271667.2:c.425-4G>A	NP_001258596.1:n.425-4G>A
NM_001271668.2:c.617-4G>A	NP_001258597.1:n.617-4G>A
NM_001271669.2:c.563-4G>A	NP_001258598.1:n.563-4G>A
NR_036448.3:n.966-4G>A