Canonical Allele Identifier: CA2710986933

Gene: DTNBP1

Linked Data

• dbSNP Id: rs2113739136

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627473del , CM000668.2:g.15627473del	GRCh38
NC_000006.11:g.15627704del , CM000668.1:g.15627704del	GRCh37
NC_000006.10:g.15735683del	NCBI36
NG_009309.1:g.40569del , LRG_588:g.40569del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.226del MANE Select	ENSP00000341680.6:p.Val76TrpfsTer?
ENST00000338950.9:c.226del	ENSP00000344718.5:p.Val76TrpfsTer?
ENST00000344537.9:c.226del	ENSP00000341680.5:p.Val76TrpfsTer?
ENST00000355917.7:c.175del	ENSP00000348183.4:p.Val59TrpfsTer?
ENST00000506844.1:c.*224del	ENSP00000424202.1:n.*224del
ENST00000510395.5:c.*136del	ENSP00000424685.1:n.*136del
ENST00000511762.2:c.121del	ENSP00000427473.2:p.Val41TrpfsTer?
ENST00000513680.5:c.*224del	ENSP00000424357.1:n.*224del
ENST00000515875.5:c.175del	ENSP00000425495.1:p.Val59TrpfsTer?
ENST00000622898.4:c.121del	ENSP00000481997.1:p.Val41TrpfsTer?
NM_001271667.1:c.-18del	NP_001258596.1:n.-18del
NM_001271668.1:c.175del	NP_001258597.1:p.Val59TrpfsTer?
NM_001271669.1:c.121del	NP_001258598.1:p.Val41TrpfsTer?
NM_032122.4:c.226del , LRG_588t1:c.226del	NP_115498.2:p.Val76TrpfsTer?
NM_183040.2:c.226del , LRG_588t2:c.226del	NP_898861.1:p.Val76TrpfsTer?
NR_036448.1:n.554del
XM_005249447.3:c.187del	XP_005249504.1:p.Val63TrpfsTer?
XM_011514936.1:c.136del	XP_011513238.1:p.Val46TrpfsTer?
XM_005249447.4:c.187del	XP_005249504.1:p.Val63TrpfsTer?
XM_011514936.3:c.136del	XP_011513238.1:p.Val46TrpfsTer?
NM_032122.5:c.226del MANE Select	NP_115498.2:p.Val76TrpfsTer?
NR_036448.2:n.524del
NM_001271667.2:c.-18del	NP_001258596.1:n.-18del
NM_001271668.2:c.175del	NP_001258597.1:p.Val59TrpfsTer?
NM_001271669.2:c.121del	NP_001258598.1:p.Val41TrpfsTer?
NR_036448.3:n.524del