Canonical Allele Identifier: CA384413119

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757222C>G (hg19) ; chr12:g.40363420C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363420C>G , CM000674.2:g.40363420C>G	GRCh38
NC_000012.11:g.40757222C>G , CM000674.1:g.40757222C>G	GRCh37
NC_000012.10:g.39043489C>G	NCBI36
NG_011709.1:g.143410C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7047C>G MANE Select	ENSP00000298910.7:p.Phe2349Leu
ENST00000636518.1:c.844C>G
ENST00000679360.1:c.*5956C>G	ENSP00000505368.1:n.*5956C>G
ENST00000679532.1:c.2821C>G
ENST00000679683.1:c.837C>G
ENST00000680018.1:c.2492C>G	ENSP00000505347.1:n.2492C>G
ENST00000680422.1:c.4134C>G
ENST00000680425.1:c.2214C>G	ENSP00000506459.1:n.2214C>G
ENST00000680453.1:c.2504C>G
ENST00000680790.1:c.6792C>G	ENSP00000505335.1:p.Phe2264Leu
ENST00000681136.1:n.3031C>G
ENST00000681696.1:c.2730C>G	ENSP00000505871.1:p.Phe910Leu
ENST00000681773.1:n.254C>G
ENST00000298910.11:c.7047C>G	ENSP00000298910.7:p.Phe2349Leu
ENST00000430804.5:c.4343C>G
ENST00000479187.5:n.3728C>G
NM_198578.3:c.7047C>G	NP_940980.3:p.Phe2349Leu
XM_005268629.2:c.7047C>G	XP_005268686.1:p.Phe2349Leu
XM_011537877.1:c.7047C>G	XP_011536179.1:p.Phe2349Leu
XM_011537879.1:c.5844C>G	XP_011536181.1:p.Phe1948Leu
XR_944868.1:n.485-8593G>C
XM_005268629.4:c.7047C>G	XP_005268686.1:p.Phe2349Leu
XM_011537877.3:c.7047C>G	XP_011536179.1:p.Phe2349Leu
XM_017018787.1:c.3963C>G	XP_016874276.1:p.Phe1321Leu
XM_017018788.2:c.3309C>G	XP_016874277.1:p.Phe1103Leu
XM_024448833.1:c.5844C>G	XP_024304601.1:p.Phe1948Leu
XR_944868.2:n.485-8593G>C
NM_198578.4:c.7047C>G MANE Select	NP_940980.4:p.Phe2349Leu