Canonical Allele Identifier: CA362869059
Gene: DTNBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15627448A>T , CM000668.2:g.15627448A>T GRCh38
NC_000006.11:g.15627679A>T , CM000668.1:g.15627679A>T GRCh37
NC_000006.10:g.15735658A>T NCBI36
NG_009309.1:g.40593T>A , LRG_588:g.40593T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344537.10:c.250T>A MANE Select ENSP00000341680.6:p.Ser84Thr
ENST00000338950.9:c.250T>A ENSP00000344718.5:p.Ser84Thr
ENST00000344537.9:c.250T>A ENSP00000341680.5:p.Ser84Thr
ENST00000355917.7:c.199T>A ENSP00000348183.4:p.Ser67Thr
ENST00000506844.1:c.*248T>A ENSP00000424202.1:n.*248T>A
ENST00000510395.5:c.*160T>A ENSP00000424685.1:n.*160T>A
ENST00000511762.2:c.145T>A ENSP00000427473.2:p.Ser49Thr
ENST00000513680.5:c.*248T>A ENSP00000424357.1:n.*248T>A
ENST00000515875.5:c.199T>A ENSP00000425495.1:p.Ser67Thr
ENST00000622898.4:c.145T>A ENSP00000481997.1:p.Ser49Thr
NM_001271667.1:c.7T>A NP_001258596.1:p.Ser3Thr
NM_001271668.1:c.199T>A NP_001258597.1:p.Ser67Thr
NM_001271669.1:c.145T>A NP_001258598.1:p.Ser49Thr
NM_032122.4:c.250T>A , LRG_588t1:c.250T>A NP_115498.2:p.Ser84Thr
NM_183040.2:c.250T>A , LRG_588t2:c.250T>A NP_898861.1:p.Ser84Thr
NR_036448.1:n.578T>A
XM_005249447.3:c.211T>A XP_005249504.1:p.Ser71Thr
XM_011514936.1:c.160T>A XP_011513238.1:p.Ser54Thr
XM_005249447.4:c.211T>A XP_005249504.1:p.Ser71Thr
XM_011514936.3:c.160T>A XP_011513238.1:p.Ser54Thr
NM_032122.5:c.250T>A MANE Select NP_115498.2:p.Ser84Thr
NR_036448.2:n.548T>A
NM_001271667.2:c.7T>A NP_001258596.1:p.Ser3Thr
NM_001271668.2:c.199T>A NP_001258597.1:p.Ser67Thr
NM_001271669.2:c.145T>A NP_001258598.1:p.Ser49Thr
NR_036448.3:n.548T>A