Canonical Allele Identifier: CA362869108
Gene: DTNBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15627469C>T , CM000668.2:g.15627469C>T GRCh38
NC_000006.11:g.15627700C>T , CM000668.1:g.15627700C>T GRCh37
NC_000006.10:g.15735679C>T NCBI36
NG_009309.1:g.40572G>A , LRG_588:g.40572G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344537.10:c.229G>A MANE Select ENSP00000341680.6:p.Asp77Asn
ENST00000338950.9:c.229G>A ENSP00000344718.5:p.Asp77Asn
ENST00000344537.9:c.229G>A ENSP00000341680.5:p.Asp77Asn
ENST00000355917.7:c.178G>A ENSP00000348183.4:p.Asp60Asn
ENST00000506844.1:c.*227G>A ENSP00000424202.1:n.*227G>A
ENST00000510395.5:c.*139G>A ENSP00000424685.1:n.*139G>A
ENST00000511762.2:c.124G>A ENSP00000427473.2:p.Asp42Asn
ENST00000513680.5:c.*227G>A ENSP00000424357.1:n.*227G>A
ENST00000515875.5:c.178G>A ENSP00000425495.1:p.Asp60Asn
ENST00000622898.4:c.124G>A ENSP00000481997.1:p.Asp42Asn
NM_001271667.1:c.-15G>A NP_001258596.1:n.-15G>A
NM_001271668.1:c.178G>A NP_001258597.1:p.Asp60Asn
NM_001271669.1:c.124G>A NP_001258598.1:p.Asp42Asn
NM_032122.4:c.229G>A , LRG_588t1:c.229G>A NP_115498.2:p.Asp77Asn
NM_183040.2:c.229G>A , LRG_588t2:c.229G>A NP_898861.1:p.Asp77Asn
NR_036448.1:n.557G>A
XM_005249447.3:c.190G>A XP_005249504.1:p.Asp64Asn
XM_011514936.1:c.139G>A XP_011513238.1:p.Asp47Asn
XM_005249447.4:c.190G>A XP_005249504.1:p.Asp64Asn
XM_011514936.3:c.139G>A XP_011513238.1:p.Asp47Asn
NM_032122.5:c.229G>A MANE Select NP_115498.2:p.Asp77Asn
NR_036448.2:n.527G>A
NM_001271667.2:c.-15G>A NP_001258596.1:n.-15G>A
NM_001271668.2:c.178G>A NP_001258597.1:p.Asp60Asn
NM_001271669.2:c.124G>A NP_001258598.1:p.Asp42Asn
NR_036448.3:n.527G>A