Canonical Allele Identifier: CA688734514

Gene: LRRK2

Linked Data

• dbSNP Id: rs1334080349
• MyVariant Identifiers: chr12:g.40757526T>C (hg19) ; chr12:g.40363724T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363724T>C , CM000674.2:g.40363724T>C	GRCh38
NC_000012.11:g.40757526T>C , CM000674.1:g.40757526T>C	GRCh37
NC_000012.10:g.39043793T>C	NCBI36
NG_011709.1:g.143714T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7181+170T>C MANE Select	ENSP00000298910.7:n.7181+170T>C
ENST00000636518.1:c.978+170T>C
ENST00000679360.1:c.*6090+170T>C	ENSP00000505368.1:n.*6090+170T>C
ENST00000679532.1:c.2955+170T>C
ENST00000679683.1:c.971+170T>C
ENST00000680018.1:c.2626+170T>C	ENSP00000505347.1:n.2626+170T>C
ENST00000680422.1:c.4268+170T>C
ENST00000680425.1:c.2348+170T>C	ENSP00000506459.1:n.2348+170T>C
ENST00000680453.1:c.2638+170T>C
ENST00000680790.1:c.6926+170T>C	ENSP00000505335.1:n.6926+170T>C
ENST00000681136.1:n.3165+170T>C
ENST00000681696.1:c.2864+170T>C	ENSP00000505871.1:n.2864+170T>C
ENST00000681773.1:n.388+170T>C
ENST00000298910.11:c.7181+170T>C	ENSP00000298910.7:n.7181+170T>C
ENST00000430804.5:c.4477+170T>C
ENST00000479187.5:n.3862+170T>C
NM_198578.3:c.7181+170T>C	NP_940980.3:n.7181+170T>C
XM_005268629.2:c.7181+170T>C	XP_005268686.1:n.7181+170T>C
XM_011537877.1:c.7181+170T>C	XP_011536179.1:n.7181+170T>C
XM_011537879.1:c.5978+170T>C	XP_011536181.1:n.5978+170T>C
XR_944868.1:n.485-8897A>G
XM_005268629.4:c.7181+170T>C	XP_005268686.1:n.7181+170T>C
XM_011537877.3:c.7181+170T>C	XP_011536179.1:n.7181+170T>C
XM_017018787.1:c.4097+170T>C	XP_016874276.1:n.4097+170T>C
XM_017018788.2:c.3443+170T>C	XP_016874277.1:n.3443+170T>C
XM_024448833.1:c.5978+170T>C	XP_024304601.1:n.5978+170T>C
XR_944868.2:n.485-8897A>G
NM_198578.4:c.7181+170T>C MANE Select	NP_940980.4:n.7181+170T>C