Canonical Allele Identifier: CA384404074

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734224G>C (hg19) ; chr12:g.40340422G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340422G>C , CM000674.2:g.40340422G>C	GRCh38
NC_000012.11:g.40734224G>C , CM000674.1:g.40734224G>C	GRCh37
NC_000012.10:g.39020491G>C	NCBI36
NG_011709.1:g.120412G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.6077G>C MANE Select	ENSP00000298910.7:p.Arg2026Thr
ENST00000679360.1:c.*4986G>C	ENSP00000505368.1:n.*4986G>C
ENST00000679532.1:c.1851G>C
ENST00000680018.1:c.1522G>C	ENSP00000505347.1:n.1522G>C
ENST00000680422.1:c.1722G>C
ENST00000680425.1:c.1244G>C	ENSP00000506459.1:n.1244G>C
ENST00000680453.1:c.1534G>C
ENST00000680790.1:c.5822G>C	ENSP00000505335.1:p.Arg1941Thr
ENST00000681136.1:n.2061G>C
ENST00000681696.1:c.1760G>C	ENSP00000505871.1:p.Arg587Thr
ENST00000298910.11:c.6077G>C	ENSP00000298910.7:p.Arg2026Thr
ENST00000430804.5:c.3373G>C
ENST00000479187.5:n.2758G>C
NM_198578.3:c.6077G>C	NP_940980.3:p.Arg2026Thr
XM_005268629.2:c.6077G>C	XP_005268686.1:p.Arg2026Thr
XM_011537877.1:c.6077G>C	XP_011536179.1:p.Arg2026Thr
XM_011537878.1:c.6077G>C	XP_011536180.1:p.Arg2026Thr
XM_011537879.1:c.4874G>C	XP_011536181.1:p.Arg1625Thr
XM_005268629.4:c.6077G>C	XP_005268686.1:p.Arg2026Thr
XM_011537877.3:c.6077G>C	XP_011536179.1:p.Arg2026Thr
XM_017018787.1:c.2993G>C	XP_016874276.1:p.Arg998Thr
XM_017018788.2:c.2339G>C	XP_016874277.1:p.Arg780Thr
XM_024448833.1:c.4874G>C	XP_024304601.1:p.Arg1625Thr
NM_198578.4:c.6077G>C MANE Select	NP_940980.4:p.Arg2026Thr