Canonical Allele Identifier: CA2031001326

Gene: LRRK2

Linked Data

• dbSNP Id: rs1945452695

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40323254_40323256del , CM000674.2:g.40323254_40323256del	GRCh38
NC_000012.11:g.40717056_40717058del , CM000674.1:g.40717056_40717058del	GRCh37
NC_000012.10:g.39003323_39003325del	NCBI36
NG_011709.1:g.103244_103246del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5604_5606del MANE Select	ENSP00000298910.7:p.Ile1868del
ENST00000679360.1:c.*4513_*4515del	ENSP00000505368.1:n.*4513_*4515del
ENST00000679532.1:c.1378_1380del
ENST00000680018.1:c.1049_1051del	ENSP00000505347.1:n.1049_1051del
ENST00000680422.1:c.1249_1251del
ENST00000680425.1:c.771_773del	ENSP00000506459.1:n.771_773del
ENST00000680453.1:c.1061_1063del
ENST00000680790.1:c.5349_5351del	ENSP00000505335.1:p.Ile1783del
ENST00000681136.1:n.1588_1590del
ENST00000681696.1:c.1287_1289del	ENSP00000505871.1:p.Ile429del
ENST00000298910.11:c.5604_5606del	ENSP00000298910.7:p.Ile1868del
ENST00000430804.5:c.2900_2902del
ENST00000479187.5:n.2285_2287del
NM_198578.3:c.5604_5606del	NP_940980.3:p.Ile1868del
XM_005268629.2:c.5604_5606del	XP_005268686.1:p.Ile1868del
XM_011537877.1:c.5604_5606del	XP_011536179.1:p.Ile1868del
XM_011537878.1:c.5604_5606del	XP_011536180.1:p.Ile1868del
XM_011537879.1:c.4401_4403del	XP_011536181.1:p.Ile1467del
XM_005268629.4:c.5604_5606del	XP_005268686.1:p.Ile1868del
XM_011537877.3:c.5604_5606del	XP_011536179.1:p.Ile1868del
XM_017018787.1:c.2520_2522del	XP_016874276.1:p.Ile840del
XM_017018788.2:c.1866_1868del	XP_016874277.1:p.Ile622del
XM_024448833.1:c.4401_4403del	XP_024304601.1:p.Ile1467del
NM_198578.4:c.5604_5606del MANE Select	NP_940980.4:p.Ile1868del