Canonical Allele Identifier: CA479238575

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40340360-G-A
• MyVariant Identifiers: chr12:g.40734162G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340360G>A , CM000674.2:g.40340360G>A	GRCh38
NC_000012.11:g.40734162G>A , CM000674.1:g.40734162G>A	GRCh37
NC_000012.10:g.39020429G>A	NCBI36
NG_011709.1:g.120350G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6015G>A MANE Select	ENSP00000298910.7:p.Leu2005=
ENST00000679360.1:c.*4924G>A	ENSP00000505368.1:n.*4924G>A
ENST00000679532.1:c.1789G>A
ENST00000680018.1:c.1460G>A	ENSP00000505347.1:n.1460G>A
ENST00000680422.1:c.1660G>A
ENST00000680425.1:c.1182G>A	ENSP00000506459.1:n.1182G>A
ENST00000680453.1:c.1472G>A
ENST00000680790.1:c.5760G>A	ENSP00000505335.1:p.Leu1920=
ENST00000681136.1:n.1999G>A
ENST00000681696.1:c.1698G>A	ENSP00000505871.1:p.Leu566=
ENST00000298910.11:c.6015G>A	ENSP00000298910.7:p.Leu2005=
ENST00000430804.5:c.3311G>A
ENST00000479187.5:n.2696G>A
NM_198578.3:c.6015G>A	NP_940980.3:p.Leu2005=
XM_005268629.2:c.6015G>A	XP_005268686.1:p.Leu2005=
XM_011537877.1:c.6015G>A	XP_011536179.1:p.Leu2005=
XM_011537878.1:c.6015G>A	XP_011536180.1:p.Leu2005=
XM_011537879.1:c.4812G>A	XP_011536181.1:p.Leu1604=
XM_005268629.4:c.6015G>A	XP_005268686.1:p.Leu2005=
XM_011537877.3:c.6015G>A	XP_011536179.1:p.Leu2005=
XM_017018787.1:c.2931G>A	XP_016874276.1:p.Leu977=
XM_017018788.2:c.2277G>A	XP_016874277.1:p.Leu759=
XM_024448833.1:c.4812G>A	XP_024304601.1:p.Leu1604=
NM_198578.4:c.6015G>A MANE Select	NP_940980.4:p.Leu2005=