Canonical Allele Identifier: CA650529904
Gene: DTNBP1 HGNC NCBI

Linked Data

dbSNP Id: rs1759420544

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15627516del , CM000668.2:g.15627516del GRCh38
NC_000006.11:g.15627747del , CM000668.1:g.15627747del GRCh37
NC_000006.10:g.15735726del NCBI36
NG_009309.1:g.40528del , LRG_588:g.40528del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344537.10:c.223-38del MANE Select ENSP00000341680.6:n.223-38del
ENST00000338950.9:c.223-38del ENSP00000344718.5:n.223-38del
ENST00000344537.9:c.223-38del ENSP00000341680.5:n.223-38del
ENST00000355917.7:c.172-38del ENSP00000348183.4:n.172-38del
ENST00000506844.1:c.*221-38del ENSP00000424202.1:n.*221-38del
ENST00000510395.5:c.*133-38del ENSP00000424685.1:n.*133-38del
ENST00000511762.2:c.118-38del ENSP00000427473.2:n.118-38del
ENST00000513680.5:c.*221-38del ENSP00000424357.1:n.*221-38del
ENST00000515875.5:c.172-38del ENSP00000425495.1:n.172-38del
ENST00000622898.4:c.118-38del ENSP00000481997.1:n.118-38del
NM_001271667.1:c.-21-38del NP_001258596.1:n.-21-38del
NM_001271668.1:c.172-38del NP_001258597.1:n.172-38del
NM_001271669.1:c.118-38del NP_001258598.1:n.118-38del
NM_032122.4:c.223-38del , LRG_588t1:c.223-38del NP_115498.2:n.223-38del
NM_183040.2:c.223-38del , LRG_588t2:c.223-38del NP_898861.1:n.223-38del
NR_036448.1:n.551-38del
XM_005249447.3:c.184-38del XP_005249504.1:n.184-38del
XM_011514936.1:c.133-38del XP_011513238.1:n.133-38del
XM_005249447.4:c.184-38del XP_005249504.1:n.184-38del
XM_011514936.3:c.133-38del XP_011513238.1:n.133-38del
NM_032122.5:c.223-38del MANE Select NP_115498.2:n.223-38del
NR_036448.2:n.521-38del
NM_001271667.2:c.-21-38del NP_001258596.1:n.-21-38del
NM_001271668.2:c.172-38del NP_001258597.1:n.172-38del
NM_001271669.2:c.118-38del NP_001258598.1:n.118-38del
NR_036448.3:n.521-38del