Canonical Allele Identifier: CA384413651

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757356G>C (hg19) ; chr12:g.40363554G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363554G>C , CM000674.2:g.40363554G>C	GRCh38
NC_000012.11:g.40757356G>C , CM000674.1:g.40757356G>C	GRCh37
NC_000012.10:g.39043623G>C	NCBI36
NG_011709.1:g.143544G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7181G>C MANE Select	ENSP00000298910.7:p.Arg2394Thr
ENST00000636518.1:c.978G>C
ENST00000679360.1:c.*6090G>C	ENSP00000505368.1:n.*6090G>C
ENST00000679532.1:c.2955G>C
ENST00000679683.1:c.971G>C
ENST00000680018.1:c.2626G>C	ENSP00000505347.1:n.2626G>C
ENST00000680422.1:c.4268G>C
ENST00000680425.1:c.2348G>C	ENSP00000506459.1:n.2348G>C
ENST00000680453.1:c.2638G>C
ENST00000680790.1:c.6926G>C	ENSP00000505335.1:p.Arg2309Thr
ENST00000681136.1:n.3165G>C
ENST00000681696.1:c.2864G>C	ENSP00000505871.1:p.Arg955Thr
ENST00000681773.1:n.388G>C
ENST00000298910.11:c.7181G>C	ENSP00000298910.7:p.Arg2394Thr
ENST00000430804.5:c.4477G>C
ENST00000479187.5:n.3862G>C
NM_198578.3:c.7181G>C	NP_940980.3:p.Arg2394Thr
XM_005268629.2:c.7181G>C	XP_005268686.1:p.Arg2394Thr
XM_011537877.1:c.7181G>C	XP_011536179.1:p.Arg2394Thr
XM_011537879.1:c.5978G>C	XP_011536181.1:p.Arg1993Thr
XR_944868.1:n.485-8727C>G
XM_005268629.4:c.7181G>C	XP_005268686.1:p.Arg2394Thr
XM_011537877.3:c.7181G>C	XP_011536179.1:p.Arg2394Thr
XM_017018787.1:c.4097G>C	XP_016874276.1:p.Arg1366Thr
XM_017018788.2:c.3443G>C	XP_016874277.1:p.Arg1148Thr
XM_024448833.1:c.5978G>C	XP_024304601.1:p.Arg1993Thr
XR_944868.2:n.485-8727C>G
NM_198578.4:c.7181G>C MANE Select	NP_940980.4:p.Arg2394Thr