Canonical Allele Identifier: CA1612347652
Gene: DTNBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15627800_15627803delinsAAAC , CM000668.2:g.15627800_15627803delinsAAAC GRCh38
NC_000006.11:g.15628031_15628034delinsAAAC , CM000668.1:g.15628031_15628034delinsAAAC GRCh37
NC_000006.10:g.15736010_15736013delinsAAAC NCBI36
NG_009309.1:g.40238_40241delinsGTTT , LRG_588:g.40238_40241delinsGTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000344537.10:c.223-328_223-325delinsGTTT MANE Select ENSP00000341680.6:n.223-328_223-325delins...
ENST00000338950.9:c.223-328_223-325delinsGTTT ENSP00000344718.5:n.223-328_223-325delins...
ENST00000344537.9:c.223-328_223-325delinsGTTT ENSP00000341680.5:n.223-328_223-325delins...
ENST00000355917.7:c.172-328_172-325delinsGTTT ENSP00000348183.4:n.172-328_172-325delins...
ENST00000506844.1:c.*221-328_*221-325delinsGTTT ENSP00000424202.1:n.*221-328_*221-325deli...
ENST00000510395.5:c.*133-328_*133-325delinsGTTT ENSP00000424685.1:n.*133-328_*133-325deli...
ENST00000511762.2:c.118-328_118-325delinsGTTT ENSP00000427473.2:n.118-328_118-325delins...
ENST00000513680.5:c.*221-328_*221-325delinsGTTT ENSP00000424357.1:n.*221-328_*221-325deli...
ENST00000515875.5:c.172-328_172-325delinsGTTT ENSP00000425495.1:n.172-328_172-325delins...
ENST00000622898.4:c.118-328_118-325delinsGTTT ENSP00000481997.1:n.118-328_118-325delins...
NM_001271667.1:c.-21-328_-21-325delinsGTTT NP_001258596.1:n.-21-328_-21-325delinsGTT...
NM_001271668.1:c.172-328_172-325delinsGTTT NP_001258597.1:n.172-328_172-325delinsGTT...
NM_001271669.1:c.118-328_118-325delinsGTTT NP_001258598.1:n.118-328_118-325delinsGTT...
NM_032122.4:c.223-328_223-325delinsGTTT , LRG_588t1:c.223-328_223-325delinsGTTT NP_115498.2:n.223-328_223-325delinsGTTT
NM_183040.2:c.223-328_223-325delinsGTTT , LRG_588t2:c.223-328_223-325delinsGTTT NP_898861.1:n.223-328_223-325delinsGTTT
NR_036448.1:n.551-328_551-325delinsGTTT
XM_005249447.3:c.184-328_184-325delinsGTTT XP_005249504.1:n.184-328_184-325delinsGTT...
XM_011514936.1:c.133-328_133-325delinsGTTT XP_011513238.1:n.133-328_133-325delinsGTT...
XM_005249447.4:c.184-328_184-325delinsGTTT XP_005249504.1:n.184-328_184-325delinsGTT...
XM_011514936.3:c.133-328_133-325delinsGTTT XP_011513238.1:n.133-328_133-325delinsGTT...
NM_032122.5:c.223-328_223-325delinsGTTT MANE Select NP_115498.2:n.223-328_223-325delinsGTTT
NR_036448.2:n.521-328_521-325delinsGTTT
NM_001271667.2:c.-21-328_-21-325delinsGTTT NP_001258596.1:n.-21-328_-21-325delinsGTT...
NM_001271668.2:c.172-328_172-325delinsGTTT NP_001258597.1:n.172-328_172-325delinsGTT...
NM_001271669.2:c.118-328_118-325delinsGTTT NP_001258598.1:n.118-328_118-325delinsGTT...
NR_036448.3:n.521-328_521-325delinsGTTT