Canonical Allele Identifier: CA2618286041

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40351511-CTGTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351516_40351520del , CM000674.2:g.40351516_40351520del	GRCh38
NC_000012.11:g.40745318_40745322del , CM000674.1:g.40745318_40745322del	GRCh37
NC_000012.10:g.39031585_39031589del	NCBI36
NG_011709.1:g.131506_131510del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6382-23_6382-19del MANE Select	ENSP00000298910.7:n.6382-23_6382-19del
ENST00000636518.1:c.179-23_179-19del
ENST00000679360.1:c.*5291-23_*5291-19del	ENSP00000505368.1:n.*5291-23_*5291-19del
ENST00000679532.1:c.2156-23_2156-19del
ENST00000679683.1:c.172-23_172-19del
ENST00000680018.1:c.1827-23_1827-19del	ENSP00000505347.1:n.1827-23_1827-19del
ENST00000680422.1:c.2027-23_2027-19del
ENST00000680425.1:c.1549-23_1549-19del	ENSP00000506459.1:n.1549-23_1549-19del
ENST00000680453.1:c.1839-23_1839-19del
ENST00000680790.1:c.6127-23_6127-19del	ENSP00000505335.1:n.6127-23_6127-19del
ENST00000681136.1:n.2366-23_2366-19del
ENST00000681696.1:c.2065-23_2065-19del	ENSP00000505871.1:n.2065-23_2065-19del
ENST00000298910.11:c.6382-23_6382-19del	ENSP00000298910.7:n.6382-23_6382-19del
ENST00000430804.5:c.3678-23_3678-19del
ENST00000479187.5:n.3063-23_3063-19del
NM_198578.3:c.6382-23_6382-19del	NP_940980.3:n.6382-23_6382-19del
XM_005268629.2:c.6382-23_6382-19del	XP_005268686.1:n.6382-23_6382-19del
XM_011537877.1:c.6382-23_6382-19del	XP_011536179.1:n.6382-23_6382-19del
XM_011537878.1:c.6382-23_6382-19del	XP_011536180.1:n.6382-23_6382-19del
XM_011537879.1:c.5179-23_5179-19del	XP_011536181.1:n.5179-23_5179-19del
XM_005268629.4:c.6382-23_6382-19del	XP_005268686.1:n.6382-23_6382-19del
XM_011537877.3:c.6382-23_6382-19del	XP_011536179.1:n.6382-23_6382-19del
XM_017018787.1:c.3298-23_3298-19del	XP_016874276.1:n.3298-23_3298-19del
XM_017018788.2:c.2644-23_2644-19del	XP_016874277.1:n.2644-23_2644-19del
XM_024448833.1:c.5179-23_5179-19del	XP_024304601.1:n.5179-23_5179-19del
NM_198578.4:c.6382-23_6382-19del MANE Select	NP_940980.4:n.6382-23_6382-19del