Canonical Allele Identifier: CA2578535000
Gene: DTNBP1 HGNC NCBI

Linked Data

gnomAD v4: 6-15627314-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15627314G>C , CM000668.2:g.15627314G>C GRCh38
NC_000006.11:g.15627545G>C , CM000668.1:g.15627545G>C GRCh37
NC_000006.10:g.15735524G>C NCBI36
NG_009309.1:g.40727C>G , LRG_588:g.40727C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344537.10:c.355+29C>G MANE Select ENSP00000341680.6:n.355+29C>G
ENST00000338950.9:c.355+29C>G ENSP00000344718.5:n.355+29C>G
ENST00000344537.9:c.355+29C>G ENSP00000341680.5:n.355+29C>G
ENST00000355917.7:c.304+29C>G ENSP00000348183.4:n.304+29C>G
ENST00000506844.1:c.*353+29C>G ENSP00000424202.1:n.*353+29C>G
ENST00000510395.5:c.*265+29C>G ENSP00000424685.1:n.*265+29C>G
ENST00000511762.2:c.250+29C>G ENSP00000427473.2:n.250+29C>G
ENST00000513680.5:c.*353+29C>G ENSP00000424357.1:n.*353+29C>G
ENST00000515875.5:c.304+29C>G ENSP00000425495.1:n.304+29C>G
ENST00000622898.4:c.250+29C>G ENSP00000481997.1:n.250+29C>G
NM_001271667.1:c.112+29C>G NP_001258596.1:n.112+29C>G
NM_001271668.1:c.304+29C>G NP_001258597.1:n.304+29C>G
NM_001271669.1:c.250+29C>G NP_001258598.1:n.250+29C>G
NM_032122.4:c.355+29C>G , LRG_588t1:c.355+29C>G NP_115498.2:n.355+29C>G
NM_183040.2:c.355+29C>G , LRG_588t2:c.355+29C>G NP_898861.1:n.355+29C>G
NR_036448.1:n.683+29C>G
XM_005249447.3:c.316+29C>G XP_005249504.1:n.316+29C>G
XM_011514936.1:c.265+29C>G XP_011513238.1:n.265+29C>G
XM_005249447.4:c.316+29C>G XP_005249504.1:n.316+29C>G
XM_011514936.3:c.265+29C>G XP_011513238.1:n.265+29C>G
NM_032122.5:c.355+29C>G MANE Select NP_115498.2:n.355+29C>G
NR_036448.2:n.653+29C>G
NM_001271667.2:c.112+29C>G NP_001258596.1:n.112+29C>G
NM_001271668.2:c.304+29C>G NP_001258597.1:n.304+29C>G
NM_001271669.2:c.250+29C>G NP_001258598.1:n.250+29C>G
NR_036448.3:n.653+29C>G