Canonical Allele Identifier: CA362869019
Gene: DTNBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15627432T>A , CM000668.2:g.15627432T>A GRCh38
NC_000006.11:g.15627663T>A , CM000668.1:g.15627663T>A GRCh37
NC_000006.10:g.15735642T>A NCBI36
NG_009309.1:g.40609A>T , LRG_588:g.40609A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344537.10:c.266A>T MANE Select ENSP00000341680.6:p.Lys89Met
ENST00000338950.9:c.266A>T ENSP00000344718.5:p.Lys89Met
ENST00000344537.9:c.266A>T ENSP00000341680.5:p.Lys89Met
ENST00000355917.7:c.215A>T ENSP00000348183.4:p.Lys72Met
ENST00000506844.1:c.*264A>T ENSP00000424202.1:n.*264A>T
ENST00000510395.5:c.*176A>T ENSP00000424685.1:n.*176A>T
ENST00000511762.2:c.161A>T ENSP00000427473.2:p.Lys54Met
ENST00000513680.5:c.*264A>T ENSP00000424357.1:n.*264A>T
ENST00000515875.5:c.215A>T ENSP00000425495.1:p.Lys72Met
ENST00000622898.4:c.161A>T ENSP00000481997.1:p.Lys54Met
NM_001271667.1:c.23A>T NP_001258596.1:p.Lys8Met
NM_001271668.1:c.215A>T NP_001258597.1:p.Lys72Met
NM_001271669.1:c.161A>T NP_001258598.1:p.Lys54Met
NM_032122.4:c.266A>T , LRG_588t1:c.266A>T NP_115498.2:p.Lys89Met
NM_183040.2:c.266A>T , LRG_588t2:c.266A>T NP_898861.1:p.Lys89Met
NR_036448.1:n.594A>T
XM_005249447.3:c.227A>T XP_005249504.1:p.Lys76Met
XM_011514936.1:c.176A>T XP_011513238.1:p.Lys59Met
XM_005249447.4:c.227A>T XP_005249504.1:p.Lys76Met
XM_011514936.3:c.176A>T XP_011513238.1:p.Lys59Met
NM_032122.5:c.266A>T MANE Select NP_115498.2:p.Lys89Met
NR_036448.2:n.564A>T
NM_001271667.2:c.23A>T NP_001258596.1:p.Lys8Met
NM_001271668.2:c.215A>T NP_001258597.1:p.Lys72Met
NM_001271669.2:c.161A>T NP_001258598.1:p.Lys54Met
NR_036448.3:n.564A>T