Canonical Allele Identifier: CA362869118
Gene: DTNBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15627475G>T , CM000668.2:g.15627475G>T GRCh38
NC_000006.11:g.15627706G>T , CM000668.1:g.15627706G>T GRCh37
NC_000006.10:g.15735685G>T NCBI36
NG_009309.1:g.40566C>A , LRG_588:g.40566C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344537.10:c.223C>A MANE Select ENSP00000341680.6:p.Leu75Met
ENST00000338950.9:c.223C>A ENSP00000344718.5:p.Leu75Met
ENST00000344537.9:c.223C>A ENSP00000341680.5:p.Leu75Met
ENST00000355917.7:c.172C>A ENSP00000348183.4:p.Leu58Met
ENST00000506844.1:c.*221C>A ENSP00000424202.1:n.*221C>A
ENST00000510395.5:c.*133C>A ENSP00000424685.1:n.*133C>A
ENST00000511762.2:c.118C>A ENSP00000427473.2:p.Leu40Met
ENST00000513680.5:c.*221C>A ENSP00000424357.1:n.*221C>A
ENST00000515875.5:c.172C>A ENSP00000425495.1:p.Leu58Met
ENST00000622898.4:c.118C>A ENSP00000481997.1:p.Leu40Met
NM_001271667.1:c.-21C>A NP_001258596.1:n.-21C>A
NM_001271668.1:c.172C>A NP_001258597.1:p.Leu58Met
NM_001271669.1:c.118C>A NP_001258598.1:p.Leu40Met
NM_032122.4:c.223C>A , LRG_588t1:c.223C>A NP_115498.2:p.Leu75Met
NM_183040.2:c.223C>A , LRG_588t2:c.223C>A NP_898861.1:p.Leu75Met
NR_036448.1:n.551C>A
XM_005249447.3:c.184C>A XP_005249504.1:p.Leu62Met
XM_011514936.1:c.133C>A XP_011513238.1:p.Leu45Met
XM_005249447.4:c.184C>A XP_005249504.1:p.Leu62Met
XM_011514936.3:c.133C>A XP_011513238.1:p.Leu45Met
NM_032122.5:c.223C>A MANE Select NP_115498.2:p.Leu75Met
NR_036448.2:n.521C>A
NM_001271667.2:c.-21C>A NP_001258596.1:n.-21C>A
NM_001271668.2:c.172C>A NP_001258597.1:p.Leu58Met
NM_001271669.2:c.118C>A NP_001258598.1:p.Leu40Met
NR_036448.3:n.521C>A