Canonical Allele Identifier: CA2677408217
Gene: DTNBP1 HGNC NCBI

Linked Data

gnomAD v4: 6-15627307-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15627307C>T , CM000668.2:g.15627307C>T GRCh38
NC_000006.11:g.15627538C>T , CM000668.1:g.15627538C>T GRCh37
NC_000006.10:g.15735517C>T NCBI36
NG_009309.1:g.40734G>A , LRG_588:g.40734G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344537.10:c.355+36G>A MANE Select ENSP00000341680.6:n.355+36G>A
ENST00000338950.9:c.355+36G>A ENSP00000344718.5:n.355+36G>A
ENST00000344537.9:c.355+36G>A ENSP00000341680.5:n.355+36G>A
ENST00000355917.7:c.304+36G>A ENSP00000348183.4:n.304+36G>A
ENST00000506844.1:c.*353+36G>A ENSP00000424202.1:n.*353+36G>A
ENST00000510395.5:c.*265+36G>A ENSP00000424685.1:n.*265+36G>A
ENST00000511762.2:c.250+36G>A ENSP00000427473.2:n.250+36G>A
ENST00000513680.5:c.*353+36G>A ENSP00000424357.1:n.*353+36G>A
ENST00000515875.5:c.304+36G>A ENSP00000425495.1:n.304+36G>A
ENST00000622898.4:c.250+36G>A ENSP00000481997.1:n.250+36G>A
NM_001271667.1:c.112+36G>A NP_001258596.1:n.112+36G>A
NM_001271668.1:c.304+36G>A NP_001258597.1:n.304+36G>A
NM_001271669.1:c.250+36G>A NP_001258598.1:n.250+36G>A
NM_032122.4:c.355+36G>A , LRG_588t1:c.355+36G>A NP_115498.2:n.355+36G>A
NM_183040.2:c.355+36G>A , LRG_588t2:c.355+36G>A NP_898861.1:n.355+36G>A
NR_036448.1:n.683+36G>A
XM_005249447.3:c.316+36G>A XP_005249504.1:n.316+36G>A
XM_011514936.1:c.265+36G>A XP_011513238.1:n.265+36G>A
XM_005249447.4:c.316+36G>A XP_005249504.1:n.316+36G>A
XM_011514936.3:c.265+36G>A XP_011513238.1:n.265+36G>A
NM_032122.5:c.355+36G>A MANE Select NP_115498.2:n.355+36G>A
NR_036448.2:n.653+36G>A
NM_001271667.2:c.112+36G>A NP_001258596.1:n.112+36G>A
NM_001271668.2:c.304+36G>A NP_001258597.1:n.304+36G>A
NM_001271669.2:c.250+36G>A NP_001258598.1:n.250+36G>A
NR_036448.3:n.653+36G>A