Canonical Allele Identifier: CA2677408167
Gene: DTNBP1 HGNC NCBI

Linked Data

gnomAD v4: 6-15627213-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15627213T>C , CM000668.2:g.15627213T>C GRCh38
NC_000006.11:g.15627444T>C , CM000668.1:g.15627444T>C GRCh37
NC_000006.10:g.15735423T>C NCBI36
NG_009309.1:g.40828A>G , LRG_588:g.40828A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344537.10:c.355+130A>G MANE Select ENSP00000341680.6:n.355+130A>G
ENST00000338950.9:c.355+130A>G ENSP00000344718.5:n.355+130A>G
ENST00000344537.9:c.355+130A>G ENSP00000341680.5:n.355+130A>G
ENST00000355917.7:c.304+130A>G ENSP00000348183.4:n.304+130A>G
ENST00000506844.1:c.*353+130A>G ENSP00000424202.1:n.*353+130A>G
ENST00000510395.5:c.*265+130A>G ENSP00000424685.1:n.*265+130A>G
ENST00000511762.2:c.250+130A>G ENSP00000427473.2:n.250+130A>G
ENST00000513680.5:c.*353+130A>G ENSP00000424357.1:n.*353+130A>G
ENST00000515875.5:c.304+130A>G ENSP00000425495.1:n.304+130A>G
ENST00000622898.4:c.250+130A>G ENSP00000481997.1:n.250+130A>G
NM_001271667.1:c.112+130A>G NP_001258596.1:n.112+130A>G
NM_001271668.1:c.304+130A>G NP_001258597.1:n.304+130A>G
NM_001271669.1:c.250+130A>G NP_001258598.1:n.250+130A>G
NM_032122.4:c.355+130A>G , LRG_588t1:c.355+130A>G NP_115498.2:n.355+130A>G
NM_183040.2:c.355+130A>G , LRG_588t2:c.355+130A>G NP_898861.1:n.355+130A>G
NR_036448.1:n.683+130A>G
XM_005249447.3:c.316+130A>G XP_005249504.1:n.316+130A>G
XM_011514936.1:c.265+130A>G XP_011513238.1:n.265+130A>G
XM_005249447.4:c.316+130A>G XP_005249504.1:n.316+130A>G
XM_011514936.3:c.265+130A>G XP_011513238.1:n.265+130A>G
NM_032122.5:c.355+130A>G MANE Select NP_115498.2:n.355+130A>G
NR_036448.2:n.653+130A>G
NM_001271667.2:c.112+130A>G NP_001258596.1:n.112+130A>G
NM_001271668.2:c.304+130A>G NP_001258597.1:n.304+130A>G
NM_001271669.2:c.250+130A>G NP_001258598.1:n.250+130A>G
NR_036448.3:n.653+130A>G