Canonical Allele Identifier: CA479238746

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734207T>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6060T>A MANE Select	ENSP00000298910.7:p.Ile2020=
ENST00000679360.1:c.*4969T>A	ENSP00000505368.1:n.*4969T>A
ENST00000679532.1:c.1834T>A
ENST00000680018.1:c.1505T>A	ENSP00000505347.1:n.1505T>A
ENST00000680422.1:c.1705T>A
ENST00000680425.1:c.1227T>A	ENSP00000506459.1:n.1227T>A
ENST00000680453.1:c.1517T>A
ENST00000680790.1:c.5805T>A	ENSP00000505335.1:p.Ile1935=
ENST00000681136.1:n.2044T>A
ENST00000681696.1:c.1743T>A	ENSP00000505871.1:p.Ile581=
ENST00000298910.11:c.6060T>A	ENSP00000298910.7:p.Ile2020=
ENST00000430804.5:c.3356T>A
ENST00000479187.5:n.2741T>A
NM_198578.3:c.6060T>A	NP_940980.3:p.Ile2020=
XM_005268629.2:c.6060T>A	XP_005268686.1:p.Ile2020=
XM_011537877.1:c.6060T>A	XP_011536179.1:p.Ile2020=
XM_011537878.1:c.6060T>A	XP_011536180.1:p.Ile2020=
XM_011537879.1:c.4857T>A	XP_011536181.1:p.Ile1619=
XM_005268629.4:c.6060T>A	XP_005268686.1:p.Ile2020=
XM_011537877.3:c.6060T>A	XP_011536179.1:p.Ile2020=
XM_017018787.1:c.2976T>A	XP_016874276.1:p.Ile992=
XM_017018788.2:c.2322T>A	XP_016874277.1:p.Ile774=
XM_024448833.1:c.4857T>A	XP_024304601.1:p.Ile1619=
NM_198578.4:c.6060T>A MANE Select	NP_940980.4:p.Ile2020=