Canonical Allele Identifier: CA2618284237

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40320145-TAGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320148_40320150del , CM000674.2:g.40320148_40320150del	GRCh38
NC_000012.11:g.40713950_40713952del , CM000674.1:g.40713950_40713952del	GRCh37
NC_000012.10:g.39000217_39000219del	NCBI36
NG_011709.1:g.100138_100140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4988_4990del MANE Select	ENSP00000298910.7:p.Gly1663del
ENST00000679360.1:c.*3897_*3899del	ENSP00000505368.1:n.*3897_*3899del
ENST00000679532.1:c.762_764del
ENST00000680018.1:c.433_435del	ENSP00000505347.1:n.433_435del
ENST00000680422.1:c.633_635del
ENST00000680425.1:c.183-886_183-884del	ENSP00000506459.1:n.183-886_183-884del
ENST00000680453.1:c.473-886_473-884del
ENST00000680790.1:c.4733_4735del	ENSP00000505335.1:p.Gly1578del
ENST00000681136.1:n.972_974del
ENST00000681696.1:c.671_673del	ENSP00000505871.1:p.Gly224del
ENST00000298910.11:c.4988_4990del	ENSP00000298910.7:p.Gly1663del
ENST00000430804.5:c.2284_2286del
ENST00000479187.5:n.1669_1671del
NM_198578.3:c.4988_4990del	NP_940980.3:p.Gly1663del
XM_005268629.2:c.4988_4990del	XP_005268686.1:p.Gly1663del
XM_011537877.1:c.4988_4990del	XP_011536179.1:p.Gly1663del
XM_011537878.1:c.4988_4990del	XP_011536180.1:p.Gly1663del
XM_011537879.1:c.3785_3787del	XP_011536181.1:p.Gly1262del
XM_011537881.1:c.4828-886_4828-884del	XP_011536183.1:n.4828-886_4828-884del
XM_005268629.4:c.4988_4990del	XP_005268686.1:p.Gly1663del
XM_011537877.3:c.4988_4990del	XP_011536179.1:p.Gly1663del
XM_011537881.3:c.4828-886_4828-884del	XP_011536183.1:n.4828-886_4828-884del
XM_017018787.1:c.1904_1906del	XP_016874276.1:p.Gly635del
XM_017018788.2:c.1250_1252del	XP_016874277.1:p.Gly417del
XM_024448833.1:c.3785_3787del	XP_024304601.1:p.Gly1262del
XR_001748574.2:n.5356_5358del
NM_198578.4:c.4988_4990del MANE Select	NP_940980.4:p.Gly1663del