Canonical Allele Identifier: CA946827746

Gene: LRRK2

Linked Data

• dbSNP Id: rs1945359802
• gnomAD v3: 12-40320253-CTATAATAGATGTA-C
• gnomAD v4: 12-40320253-CTATAATAGATGTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320255_40320267del , CM000674.2:g.40320255_40320267del	GRCh38
NC_000012.11:g.40714057_40714069del , CM000674.1:g.40714057_40714069del	GRCh37
NC_000012.10:g.39000324_39000336del	NCBI36
NG_011709.1:g.100245_100257del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5015+80_5015+92del MANE Select	ENSP00000298910.7:n.5015+80_5015+92del
ENST00000679360.1:c.*3924+80_*3924+92del	ENSP00000505368.1:n.*3924+80_*3924+92del
ENST00000679532.1:c.789+80_789+92del
ENST00000680018.1:c.460+80_460+92del	ENSP00000505347.1:n.460+80_460+92del
ENST00000680422.1:c.660+80_660+92del
ENST00000680425.1:c.183-779_183-767del	ENSP00000506459.1:n.183-779_183-767del
ENST00000680453.1:c.473-779_473-767del
ENST00000680790.1:c.4760+80_4760+92del	ENSP00000505335.1:n.4760+80_4760+92del
ENST00000681136.1:n.999+80_999+92del
ENST00000681696.1:c.698+80_698+92del	ENSP00000505871.1:n.698+80_698+92del
ENST00000298910.11:c.5015+80_5015+92del	ENSP00000298910.7:n.5015+80_5015+92del
ENST00000430804.5:c.2311+80_2311+92del
ENST00000479187.5:n.1696+80_1696+92del
NM_198578.3:c.5015+80_5015+92del	NP_940980.3:n.5015+80_5015+92del
XM_005268629.2:c.5015+80_5015+92del	XP_005268686.1:n.5015+80_5015+92del
XM_011537877.1:c.5015+80_5015+92del	XP_011536179.1:n.5015+80_5015+92del
XM_011537878.1:c.5015+80_5015+92del	XP_011536180.1:n.5015+80_5015+92del
XM_011537879.1:c.3812+80_3812+92del	XP_011536181.1:n.3812+80_3812+92del
XM_011537881.1:c.4828-779_4828-767del	XP_011536183.1:n.4828-779_4828-767del
XM_005268629.4:c.5015+80_5015+92del	XP_005268686.1:n.5015+80_5015+92del
XM_011537877.3:c.5015+80_5015+92del	XP_011536179.1:n.5015+80_5015+92del
XM_011537881.3:c.4828-779_4828-767del	XP_011536183.1:n.4828-779_4828-767del
XM_017018787.1:c.1931+80_1931+92del	XP_016874276.1:n.1931+80_1931+92del
XM_017018788.2:c.1277+80_1277+92del	XP_016874277.1:n.1277+80_1277+92del
XM_024448833.1:c.3812+80_3812+92del	XP_024304601.1:n.3812+80_3812+92del
XR_001748574.2:n.5383+80_5383+92del
NM_198578.4:c.5015+80_5015+92del MANE Select	NP_940980.4:n.5015+80_5015+92del