Canonical Allele Identifier: CA384413554

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757329G>C (hg19) ; chr12:g.40363527G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363527G>C , CM000674.2:g.40363527G>C	GRCh38
NC_000012.11:g.40757329G>C , CM000674.1:g.40757329G>C	GRCh37
NC_000012.10:g.39043596G>C	NCBI36
NG_011709.1:g.143517G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7154G>C MANE Select	ENSP00000298910.7:p.Gly2385Ala
ENST00000636518.1:c.951G>C
ENST00000679360.1:c.*6063G>C	ENSP00000505368.1:n.*6063G>C
ENST00000679532.1:c.2928G>C
ENST00000679683.1:c.944G>C
ENST00000680018.1:c.2599G>C	ENSP00000505347.1:n.2599G>C
ENST00000680422.1:c.4241G>C
ENST00000680425.1:c.2321G>C	ENSP00000506459.1:n.2321G>C
ENST00000680453.1:c.2611G>C
ENST00000680790.1:c.6899G>C	ENSP00000505335.1:p.Gly2300Ala
ENST00000681136.1:n.3138G>C
ENST00000681696.1:c.2837G>C	ENSP00000505871.1:p.Gly946Ala
ENST00000681773.1:n.361G>C
ENST00000298910.11:c.7154G>C	ENSP00000298910.7:p.Gly2385Ala
ENST00000430804.5:c.4450G>C
ENST00000479187.5:n.3835G>C
NM_198578.3:c.7154G>C	NP_940980.3:p.Gly2385Ala
XM_005268629.2:c.7154G>C	XP_005268686.1:p.Gly2385Ala
XM_011537877.1:c.7154G>C	XP_011536179.1:p.Gly2385Ala
XM_011537879.1:c.5951G>C	XP_011536181.1:p.Gly1984Ala
XR_944868.1:n.485-8700C>G
XM_005268629.4:c.7154G>C	XP_005268686.1:p.Gly2385Ala
XM_011537877.3:c.7154G>C	XP_011536179.1:p.Gly2385Ala
XM_017018787.1:c.4070G>C	XP_016874276.1:p.Gly1357Ala
XM_017018788.2:c.3416G>C	XP_016874277.1:p.Gly1139Ala
XM_024448833.1:c.5951G>C	XP_024304601.1:p.Gly1984Ala
XR_944868.2:n.485-8700C>G
NM_198578.4:c.7154G>C MANE Select	NP_940980.4:p.Gly2385Ala