Canonical Allele Identifier: CA1612376416
Gene: DTNBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15572817_15572843delinsAACCTCCCTGACGTAAGTGATCCTCCC , CM000668.2:g.15572817_15572843delinsAACCTCCCTGACGTAAGTGATCCTCCC GRCh38
NC_000006.11:g.15573048_15573074delinsAACCTCCCTGACGTAAGTGATCCTCCC , CM000668.1:g.15573048_15573074delinsAACCTCCCTGACGTAAGTGATCCTCCC GRCh37
NC_000006.10:g.15681027_15681053delinsAACCTCCCTGACGTAAGTGATCCTCCC NCBI36
NG_009309.1:g.95198_95224delinsGGGAGGATCACTTACGTCAGGGAGGTT , LRG_588:g.95198_95224delinsGGGAGGATCACTTACGTCAGGGAGGTT

Transcript Alleles

HGVS Amino-acid change
ENST00000344537.10:c.511+20216_511+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT MANE Select ENSP00000341680.6:n.511+20216_511+20242de...
ENST00000338950.9:c.511+20216_511+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT ENSP00000344718.5:n.511+20216_511+20242de...
ENST00000344537.9:c.511+20216_511+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT ENSP00000341680.5:n.511+20216_511+20242de...
ENST00000355917.7:c.460+20216_460+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT ENSP00000348183.4:n.460+20216_460+20242de...
ENST00000462989.6:c.43+12876_43+12902delinsGGGAGGATCACTTACGTCAGGGAGGTT ENSP00000427239.1:n.43+12876_43+12902deli...
ENST00000506844.1:c.*509+20216_*509+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT ENSP00000424202.1:n.*509+20216_*509+20242...
ENST00000510395.5:c.*421+20216_*421+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT ENSP00000424685.1:n.*421+20216_*421+20242...
ENST00000511762.2:c.406+20216_406+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT ENSP00000427473.2:n.406+20216_406+20242de...
ENST00000513680.5:c.*509+20216_*509+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT ENSP00000424357.1:n.*509+20216_*509+20242...
ENST00000515875.5:c.460+20216_460+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT ENSP00000425495.1:n.460+20216_460+20242de...
ENST00000622898.4:c.406+20216_406+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT ENSP00000481997.1:n.406+20216_406+20242de...
NM_001271667.1:c.268+20216_268+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT NP_001258596.1:n.268+20216_268+20242delin...
NM_001271668.1:c.460+20216_460+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT NP_001258597.1:n.460+20216_460+20242delin...
NM_001271669.1:c.406+20216_406+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT NP_001258598.1:n.406+20216_406+20242delin...
NM_032122.4:c.511+20216_511+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT , LRG_588t1:c.511+20216_511+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT NP_115498.2:n.511+20216_511+20242delinsGG...
NM_183040.2:c.511+20216_511+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT , LRG_588t2:c.511+20216_511+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT NP_898861.1:n.511+20216_511+20242delinsGG...
NR_036448.1:n.839+20216_839+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT
XM_005249447.3:c.472+20216_472+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT XP_005249504.1:n.472+20216_472+20242delin...
XM_011514936.1:c.421+20216_421+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT XP_011513238.1:n.421+20216_421+20242delin...
XM_011514937.1:c.43+12876_43+12902delinsGGGAGGATCACTTACGTCAGGGAGGTT XP_011513239.1:n.43+12876_43+12902delinsG...
XM_005249447.4:c.472+20216_472+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT XP_005249504.1:n.472+20216_472+20242delin...
XM_011514936.3:c.421+20216_421+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT XP_011513238.1:n.421+20216_421+20242delin...
XM_011514937.2:c.43+12876_43+12902delinsGGGAGGATCACTTACGTCAGGGAGGTT XP_011513239.1:n.43+12876_43+12902delinsG...
NM_032122.5:c.511+20216_511+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT MANE Select NP_115498.2:n.511+20216_511+20242delinsGG...
NR_036448.2:n.809+20216_809+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT
NM_001271667.2:c.268+20216_268+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT NP_001258596.1:n.268+20216_268+20242delin...
NM_001271668.2:c.460+20216_460+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT NP_001258597.1:n.460+20216_460+20242delin...
NM_001271669.2:c.406+20216_406+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT NP_001258598.1:n.406+20216_406+20242delin...
NR_036448.3:n.809+20216_809+20242delinsGGGAGGATCACTTACGTCAGGGAGGTT