Canonical Allele Identifier: CA2030995570

Gene: LRRK2

Linked Data

• dbSNP Id: rs1945363336

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320358_40320363del , CM000674.2:g.40320358_40320363del	GRCh38
NC_000012.11:g.40714160_40714165del , CM000674.1:g.40714160_40714165del	GRCh37
NC_000012.10:g.39000427_39000432del	NCBI36
NG_011709.1:g.100348_100353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5015+183_5015+188del MANE Select	ENSP00000298910.7:n.5015+183_5015+188del
ENST00000679360.1:c.*3924+183_*3924+188del	ENSP00000505368.1:n.*3924+183_*3924+188del
ENST00000679532.1:c.789+183_789+188del
ENST00000680018.1:c.460+183_460+188del	ENSP00000505347.1:n.460+183_460+188del
ENST00000680422.1:c.660+183_660+188del
ENST00000680425.1:c.183-676_183-671del	ENSP00000506459.1:n.183-676_183-671del
ENST00000680453.1:c.473-676_473-671del
ENST00000680790.1:c.4760+183_4760+188del	ENSP00000505335.1:n.4760+183_4760+188del
ENST00000681136.1:n.999+183_999+188del
ENST00000681696.1:c.698+183_698+188del	ENSP00000505871.1:n.698+183_698+188del
ENST00000298910.11:c.5015+183_5015+188del	ENSP00000298910.7:n.5015+183_5015+188del
ENST00000430804.5:c.2311+183_2311+188del
ENST00000479187.5:n.1696+183_1696+188del
NM_198578.3:c.5015+183_5015+188del	NP_940980.3:n.5015+183_5015+188del
XM_005268629.2:c.5015+183_5015+188del	XP_005268686.1:n.5015+183_5015+188del
XM_011537877.1:c.5015+183_5015+188del	XP_011536179.1:n.5015+183_5015+188del
XM_011537878.1:c.5015+183_5015+188del	XP_011536180.1:n.5015+183_5015+188del
XM_011537879.1:c.3812+183_3812+188del	XP_011536181.1:n.3812+183_3812+188del
XM_011537881.1:c.4828-676_4828-671del	XP_011536183.1:n.4828-676_4828-671del
XM_005268629.4:c.5015+183_5015+188del	XP_005268686.1:n.5015+183_5015+188del
XM_011537877.3:c.5015+183_5015+188del	XP_011536179.1:n.5015+183_5015+188del
XM_011537881.3:c.4828-676_4828-671del	XP_011536183.1:n.4828-676_4828-671del
XM_017018787.1:c.1931+183_1931+188del	XP_016874276.1:n.1931+183_1931+188del
XM_017018788.2:c.1277+183_1277+188del	XP_016874277.1:n.1277+183_1277+188del
XM_024448833.1:c.3812+183_3812+188del	XP_024304601.1:n.3812+183_3812+188del
XR_001748574.2:n.5383+183_5383+188del
NM_198578.4:c.5015+183_5015+188del MANE Select	NP_940980.4:n.5015+183_5015+188del