Canonical Allele Identifier: CA384413586

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40363538-T-A
• MyVariant Identifiers: chr12:g.40757340T>A (hg19) ; chr12:g.40363538T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363538T>A , CM000674.2:g.40363538T>A	GRCh38
NC_000012.11:g.40757340T>A , CM000674.1:g.40757340T>A	GRCh37
NC_000012.10:g.39043607T>A	NCBI36
NG_011709.1:g.143528T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7165T>A MANE Select	ENSP00000298910.7:p.Cys2389Ser
ENST00000636518.1:c.962T>A
ENST00000679360.1:c.*6074T>A	ENSP00000505368.1:n.*6074T>A
ENST00000679532.1:c.2939T>A
ENST00000679683.1:c.955T>A
ENST00000680018.1:c.2610T>A	ENSP00000505347.1:n.2610T>A
ENST00000680422.1:c.4252T>A
ENST00000680425.1:c.2332T>A	ENSP00000506459.1:n.2332T>A
ENST00000680453.1:c.2622T>A
ENST00000680790.1:c.6910T>A	ENSP00000505335.1:p.Cys2304Ser
ENST00000681136.1:n.3149T>A
ENST00000681696.1:c.2848T>A	ENSP00000505871.1:p.Cys950Ser
ENST00000681773.1:n.372T>A
ENST00000298910.11:c.7165T>A	ENSP00000298910.7:p.Cys2389Ser
ENST00000430804.5:c.4461T>A
ENST00000479187.5:n.3846T>A
NM_198578.3:c.7165T>A	NP_940980.3:p.Cys2389Ser
XM_005268629.2:c.7165T>A	XP_005268686.1:p.Cys2389Ser
XM_011537877.1:c.7165T>A	XP_011536179.1:p.Cys2389Ser
XM_011537879.1:c.5962T>A	XP_011536181.1:p.Cys1988Ser
XR_944868.1:n.485-8711A>T
XM_005268629.4:c.7165T>A	XP_005268686.1:p.Cys2389Ser
XM_011537877.3:c.7165T>A	XP_011536179.1:p.Cys2389Ser
XM_017018787.1:c.4081T>A	XP_016874276.1:p.Cys1361Ser
XM_017018788.2:c.3427T>A	XP_016874277.1:p.Cys1143Ser
XM_024448833.1:c.5962T>A	XP_024304601.1:p.Cys1988Ser
XR_944868.2:n.485-8711A>T
NM_198578.4:c.7165T>A MANE Select	NP_940980.4:p.Cys2389Ser