Canonical Allele Identifier: CA384404112

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734232A>C (hg19) ; chr12:g.40340430A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340430A>C , CM000674.2:g.40340430A>C	GRCh38
NC_000012.11:g.40734232A>C , CM000674.1:g.40734232A>C	GRCh37
NC_000012.10:g.39020499A>C	NCBI36
NG_011709.1:g.120420A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6085A>C MANE Select	ENSP00000298910.7:p.Ile2029Leu
ENST00000679360.1:c.*4994A>C	ENSP00000505368.1:n.*4994A>C
ENST00000679532.1:c.1859A>C
ENST00000680018.1:c.1530A>C	ENSP00000505347.1:n.1530A>C
ENST00000680422.1:c.1730A>C
ENST00000680425.1:c.1252A>C	ENSP00000506459.1:n.1252A>C
ENST00000680453.1:c.1542A>C
ENST00000680790.1:c.5830A>C	ENSP00000505335.1:p.Ile1944Leu
ENST00000681136.1:n.2069A>C
ENST00000681696.1:c.1768A>C	ENSP00000505871.1:p.Ile590Leu
ENST00000298910.11:c.6085A>C	ENSP00000298910.7:p.Ile2029Leu
ENST00000430804.5:c.3381A>C
ENST00000479187.5:n.2766A>C
NM_198578.3:c.6085A>C	NP_940980.3:p.Ile2029Leu
XM_005268629.2:c.6085A>C	XP_005268686.1:p.Ile2029Leu
XM_011537877.1:c.6085A>C	XP_011536179.1:p.Ile2029Leu
XM_011537878.1:c.6085A>C	XP_011536180.1:p.Ile2029Leu
XM_011537879.1:c.4882A>C	XP_011536181.1:p.Ile1628Leu
XM_005268629.4:c.6085A>C	XP_005268686.1:p.Ile2029Leu
XM_011537877.3:c.6085A>C	XP_011536179.1:p.Ile2029Leu
XM_017018787.1:c.3001A>C	XP_016874276.1:p.Ile1001Leu
XM_017018788.2:c.2347A>C	XP_016874277.1:p.Ile783Leu
XM_024448833.1:c.4882A>C	XP_024304601.1:p.Ile1628Leu
NM_198578.4:c.6085A>C MANE Select	NP_940980.4:p.Ile2029Leu