Canonical Allele Identifier: CA2030995454

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320313_40320314delinsCA , CM000674.2:g.40320313_40320314delinsCA	GRCh38
NC_000012.11:g.40714115_40714116delinsCA , CM000674.1:g.40714115_40714116delinsCA	GRCh37
NC_000012.10:g.39000382_39000383delinsCA	NCBI36
NG_011709.1:g.100303_100304delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5015+138_5015+139delinsCA MANE Select	ENSP00000298910.7:n.5015+138_5015+139delinsCA
ENST00000679360.1:c.*3924+138_*3924+139delinsCA	ENSP00000505368.1:n.*3924+138_*3924+139delinsCA
ENST00000679532.1:c.789+138_789+139delinsCA
ENST00000680018.1:c.460+138_460+139delinsCA	ENSP00000505347.1:n.460+138_460+139delinsCA
ENST00000680422.1:c.660+138_660+139delinsCA
ENST00000680425.1:c.183-721_183-720delinsCA	ENSP00000506459.1:n.183-721_183-720delinsCA
ENST00000680453.1:c.473-721_473-720delinsCA
ENST00000680790.1:c.4760+138_4760+139delinsCA	ENSP00000505335.1:n.4760+138_4760+139delinsCA
ENST00000681136.1:n.999+138_999+139delinsCA
ENST00000681696.1:c.698+138_698+139delinsCA	ENSP00000505871.1:n.698+138_698+139delinsCA
ENST00000298910.11:c.5015+138_5015+139delinsCA	ENSP00000298910.7:n.5015+138_5015+139delinsCA
ENST00000430804.5:c.2311+138_2311+139delinsCA
ENST00000479187.5:n.1696+138_1696+139delinsCA
NM_198578.3:c.5015+138_5015+139delinsCA	NP_940980.3:n.5015+138_5015+139delinsCA
XM_005268629.2:c.5015+138_5015+139delinsCA	XP_005268686.1:n.5015+138_5015+139delinsCA
XM_011537877.1:c.5015+138_5015+139delinsCA	XP_011536179.1:n.5015+138_5015+139delinsCA
XM_011537878.1:c.5015+138_5015+139delinsCA	XP_011536180.1:n.5015+138_5015+139delinsCA
XM_011537879.1:c.3812+138_3812+139delinsCA	XP_011536181.1:n.3812+138_3812+139delinsCA
XM_011537881.1:c.4828-721_4828-720delinsCA	XP_011536183.1:n.4828-721_4828-720delinsCA
XM_005268629.4:c.5015+138_5015+139delinsCA	XP_005268686.1:n.5015+138_5015+139delinsCA
XM_011537877.3:c.5015+138_5015+139delinsCA	XP_011536179.1:n.5015+138_5015+139delinsCA
XM_011537881.3:c.4828-721_4828-720delinsCA	XP_011536183.1:n.4828-721_4828-720delinsCA
XM_017018787.1:c.1931+138_1931+139delinsCA	XP_016874276.1:n.1931+138_1931+139delinsCA
XM_017018788.2:c.1277+138_1277+139delinsCA	XP_016874277.1:n.1277+138_1277+139delinsCA
XM_024448833.1:c.3812+138_3812+139delinsCA	XP_024304601.1:n.3812+138_3812+139delinsCA
XR_001748574.2:n.5383+138_5383+139delinsCA
NM_198578.4:c.5015+138_5015+139delinsCA MANE Select	NP_940980.4:n.5015+138_5015+139delinsCA