Canonical Allele Identifier: CA384403995

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734207T>G (hg19) ; chr12:g.40340405T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340405T>G , CM000674.2:g.40340405T>G	GRCh38
NC_000012.11:g.40734207T>G , CM000674.1:g.40734207T>G	GRCh37
NC_000012.10:g.39020474T>G	NCBI36
NG_011709.1:g.120395T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.6060T>G MANE Select	ENSP00000298910.7:p.Ile2020Met
ENST00000679360.1:c.*4969T>G	ENSP00000505368.1:n.*4969T>G
ENST00000679532.1:c.1834T>G
ENST00000680018.1:c.1505T>G	ENSP00000505347.1:n.1505T>G
ENST00000680422.1:c.1705T>G
ENST00000680425.1:c.1227T>G	ENSP00000506459.1:n.1227T>G
ENST00000680453.1:c.1517T>G
ENST00000680790.1:c.5805T>G	ENSP00000505335.1:p.Ile1935Met
ENST00000681136.1:n.2044T>G
ENST00000681696.1:c.1743T>G	ENSP00000505871.1:p.Ile581Met
ENST00000298910.11:c.6060T>G	ENSP00000298910.7:p.Ile2020Met
ENST00000430804.5:c.3356T>G
ENST00000479187.5:n.2741T>G
NM_198578.3:c.6060T>G	NP_940980.3:p.Ile2020Met
XM_005268629.2:c.6060T>G	XP_005268686.1:p.Ile2020Met
XM_011537877.1:c.6060T>G	XP_011536179.1:p.Ile2020Met
XM_011537878.1:c.6060T>G	XP_011536180.1:p.Ile2020Met
XM_011537879.1:c.4857T>G	XP_011536181.1:p.Ile1619Met
XM_005268629.4:c.6060T>G	XP_005268686.1:p.Ile2020Met
XM_011537877.3:c.6060T>G	XP_011536179.1:p.Ile2020Met
XM_017018787.1:c.2976T>G	XP_016874276.1:p.Ile992Met
XM_017018788.2:c.2322T>G	XP_016874277.1:p.Ile774Met
XM_024448833.1:c.4857T>G	XP_024304601.1:p.Ile1619Met
NM_198578.4:c.6060T>G MANE Select	NP_940980.4:p.Ile2020Met