Canonical Allele Identifier: CA2618284233

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40320054-GAAAAATTTCTTTCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320060_40320073del , CM000674.2:g.40320060_40320073del	GRCh38
NC_000012.11:g.40713862_40713875del , CM000674.1:g.40713862_40713875del	GRCh37
NC_000012.10:g.39000129_39000142del	NCBI36
NG_011709.1:g.100050_100063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4900_4913del MANE Select	ENSP00000298910.7:p.Phe1634LysfsTer13
ENST00000679360.1:c.*3809_*3822del	ENSP00000505368.1:n.*3809_*3822del
ENST00000679532.1:c.674_687del
ENST00000680018.1:c.345_358del	ENSP00000505347.1:n.345_358del
ENST00000680422.1:c.545_558del
ENST00000680425.1:c.183-974_183-961del	ENSP00000506459.1:n.183-974_183-961del
ENST00000680453.1:c.473-974_473-961del
ENST00000680790.1:c.4645_4658del	ENSP00000505335.1:p.Phe1549LysfsTer13
ENST00000681136.1:n.884_897del
ENST00000681696.1:c.583_596del	ENSP00000505871.1:p.Phe195LysfsTer13
ENST00000298910.11:c.4900_4913del	ENSP00000298910.7:p.Phe1634LysfsTer13
ENST00000430804.5:c.2196_2209del
ENST00000479187.5:n.1581_1594del
NM_198578.3:c.4900_4913del	NP_940980.3:p.Phe1634LysfsTer13
XM_005268629.2:c.4900_4913del	XP_005268686.1:p.Phe1634LysfsTer13
XM_011537877.1:c.4900_4913del	XP_011536179.1:p.Phe1634LysfsTer13
XM_011537878.1:c.4900_4913del	XP_011536180.1:p.Phe1634LysfsTer13
XM_011537879.1:c.3697_3710del	XP_011536181.1:p.Phe1233LysfsTer13
XM_011537881.1:c.4828-974_4828-961del	XP_011536183.1:n.4828-974_4828-961del
XM_005268629.4:c.4900_4913del	XP_005268686.1:p.Phe1634LysfsTer13
XM_011537877.3:c.4900_4913del	XP_011536179.1:p.Phe1634LysfsTer13
XM_011537881.3:c.4828-974_4828-961del	XP_011536183.1:n.4828-974_4828-961del
XM_017018787.1:c.1816_1829del	XP_016874276.1:p.Phe606LysfsTer13
XM_017018788.2:c.1162_1175del	XP_016874277.1:p.Phe388LysfsTer13
XM_024448833.1:c.3697_3710del	XP_024304601.1:p.Phe1233LysfsTer13
XR_001748574.2:n.5268_5281del
NM_198578.4:c.4900_4913del MANE Select	NP_940980.4:p.Phe1634LysfsTer13