Canonical Allele Identifier: CA362868943
Gene: DTNBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15627397G>C , CM000668.2:g.15627397G>C GRCh38
NC_000006.11:g.15627628G>C , CM000668.1:g.15627628G>C GRCh37
NC_000006.10:g.15735607G>C NCBI36
NG_009309.1:g.40644C>G , LRG_588:g.40644C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344537.10:c.301C>G MANE Select ENSP00000341680.6:p.Leu101Val
ENST00000338950.9:c.301C>G ENSP00000344718.5:p.Leu101Val
ENST00000344537.9:c.301C>G ENSP00000341680.5:p.Leu101Val
ENST00000355917.7:c.250C>G ENSP00000348183.4:p.Leu84Val
ENST00000506844.1:c.*299C>G ENSP00000424202.1:n.*299C>G
ENST00000510395.5:c.*211C>G ENSP00000424685.1:n.*211C>G
ENST00000511762.2:c.196C>G ENSP00000427473.2:p.Leu66Val
ENST00000513680.5:c.*299C>G ENSP00000424357.1:n.*299C>G
ENST00000515875.5:c.250C>G ENSP00000425495.1:p.Leu84Val
ENST00000622898.4:c.196C>G ENSP00000481997.1:p.Leu66Val
NM_001271667.1:c.58C>G NP_001258596.1:p.Leu20Val
NM_001271668.1:c.250C>G NP_001258597.1:p.Leu84Val
NM_001271669.1:c.196C>G NP_001258598.1:p.Leu66Val
NM_032122.4:c.301C>G , LRG_588t1:c.301C>G NP_115498.2:p.Leu101Val
NM_183040.2:c.301C>G , LRG_588t2:c.301C>G NP_898861.1:p.Leu101Val
NR_036448.1:n.629C>G
XM_005249447.3:c.262C>G XP_005249504.1:p.Leu88Val
XM_011514936.1:c.211C>G XP_011513238.1:p.Leu71Val
XM_005249447.4:c.262C>G XP_005249504.1:p.Leu88Val
XM_011514936.3:c.211C>G XP_011513238.1:p.Leu71Val
NM_032122.5:c.301C>G MANE Select NP_115498.2:p.Leu101Val
NR_036448.2:n.599C>G
NM_001271667.2:c.58C>G NP_001258596.1:p.Leu20Val
NM_001271668.2:c.250C>G NP_001258597.1:p.Leu84Val
NM_001271669.2:c.196C>G NP_001258598.1:p.Leu66Val
NR_036448.3:n.599C>G