Canonical Allele Identifier: CA1612358278
Gene: DTNBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.15636634_15636635delinsCT , CM000668.2:g.15636634_15636635delinsCT GRCh38
NC_000006.11:g.15636865_15636866delinsCT , CM000668.1:g.15636865_15636866delinsCT GRCh37
NC_000006.10:g.15744844_15744845delinsCT NCBI36
NG_009309.1:g.31406_31407delinsAG , LRG_588:g.31406_31407delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000344537.10:c.222+1109_222+1110delinsAG MANE Select ENSP00000341680.6:n.222+1109_222+1110deli...
ENST00000338950.9:c.222+1109_222+1110delinsAG ENSP00000344718.5:n.222+1109_222+1110deli...
ENST00000344537.9:c.222+1109_222+1110delinsAG ENSP00000341680.5:n.222+1109_222+1110deli...
ENST00000355917.7:c.171+1109_171+1110delinsAG ENSP00000348183.4:n.171+1109_171+1110deli...
ENST00000506844.1:c.*220+1109_*220+1110delinsAG ENSP00000424202.1:n.*220+1109_*220+1110de...
ENST00000510395.5:c.*132+1109_*132+1110delinsAG ENSP00000424685.1:n.*132+1109_*132+1110de...
ENST00000511762.2:c.117+1109_117+1110delinsAG ENSP00000427473.2:n.117+1109_117+1110deli...
ENST00000513680.5:c.*220+1109_*220+1110delinsAG ENSP00000424357.1:n.*220+1109_*220+1110de...
ENST00000515875.5:c.171+1109_171+1110delinsAG ENSP00000425495.1:n.171+1109_171+1110deli...
ENST00000622898.4:c.117+1109_117+1110delinsAG ENSP00000481997.1:n.117+1109_117+1110deli...
NM_001271667.1:c.-22+1109_-22+1110delinsAG NP_001258596.1:n.-22+1109_-22+1110delinsA...
NM_001271668.1:c.171+1109_171+1110delinsAG NP_001258597.1:n.171+1109_171+1110delinsA...
NM_001271669.1:c.117+1109_117+1110delinsAG NP_001258598.1:n.117+1109_117+1110delinsA...
NM_032122.4:c.222+1109_222+1110delinsAG , LRG_588t1:c.222+1109_222+1110delinsAG NP_115498.2:n.222+1109_222+1110delinsAG
NM_183040.2:c.222+1109_222+1110delinsAG , LRG_588t2:c.222+1109_222+1110delinsAG NP_898861.1:n.222+1109_222+1110delinsAG
NR_036448.1:n.550+1109_550+1110delinsAG
XM_005249447.3:c.183+1109_183+1110delinsAG XP_005249504.1:n.183+1109_183+1110delinsA...
XM_011514936.1:c.132+1109_132+1110delinsAG XP_011513238.1:n.132+1109_132+1110delinsA...
XM_005249447.4:c.183+1109_183+1110delinsAG XP_005249504.1:n.183+1109_183+1110delinsA...
XM_011514936.3:c.132+1109_132+1110delinsAG XP_011513238.1:n.132+1109_132+1110delinsA...
NM_032122.5:c.222+1109_222+1110delinsAG MANE Select NP_115498.2:n.222+1109_222+1110delinsAG
NR_036448.2:n.520+1109_520+1110delinsAG
NM_001271667.2:c.-22+1109_-22+1110delinsAG NP_001258596.1:n.-22+1109_-22+1110delinsA...
NM_001271668.2:c.171+1109_171+1110delinsAG NP_001258597.1:n.171+1109_171+1110delinsA...
NM_001271669.2:c.117+1109_117+1110delinsAG NP_001258598.1:n.117+1109_117+1110delinsA...
NR_036448.3:n.520+1109_520+1110delinsAG