Canonical Allele Identifier: CA479268780

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40713969T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320167T>C , CM000674.2:g.40320167T>C	GRCh38
NC_000012.11:g.40713969T>C , CM000674.1:g.40713969T>C	GRCh37
NC_000012.10:g.39000236T>C	NCBI36
NG_011709.1:g.100157T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5007T>C MANE Select	ENSP00000298910.7:p.Val1669=
ENST00000679360.1:c.*3916T>C	ENSP00000505368.1:n.*3916T>C
ENST00000679532.1:c.781T>C
ENST00000680018.1:c.452T>C	ENSP00000505347.1:n.452T>C
ENST00000680422.1:c.652T>C
ENST00000680425.1:c.183-867T>C	ENSP00000506459.1:n.183-867T>C
ENST00000680453.1:c.473-867T>C
ENST00000680790.1:c.4752T>C	ENSP00000505335.1:p.Val1584=
ENST00000681136.1:n.991T>C
ENST00000681696.1:c.690T>C	ENSP00000505871.1:p.Val230=
ENST00000298910.11:c.5007T>C	ENSP00000298910.7:p.Val1669=
ENST00000430804.5:c.2303T>C
ENST00000479187.5:n.1688T>C
NM_198578.3:c.5007T>C	NP_940980.3:p.Val1669=
XM_005268629.2:c.5007T>C	XP_005268686.1:p.Val1669=
XM_011537877.1:c.5007T>C	XP_011536179.1:p.Val1669=
XM_011537878.1:c.5007T>C	XP_011536180.1:p.Val1669=
XM_011537879.1:c.3804T>C	XP_011536181.1:p.Val1268=
XM_011537881.1:c.4828-867T>C	XP_011536183.1:n.4828-867T>C
XM_005268629.4:c.5007T>C	XP_005268686.1:p.Val1669=
XM_011537877.3:c.5007T>C	XP_011536179.1:p.Val1669=
XM_011537881.3:c.4828-867T>C	XP_011536183.1:n.4828-867T>C
XM_017018787.1:c.1923T>C	XP_016874276.1:p.Val641=
XM_017018788.2:c.1269T>C	XP_016874277.1:p.Val423=
XM_024448833.1:c.3804T>C	XP_024304601.1:p.Val1268=
XR_001748574.2:n.5375T>C
NM_198578.4:c.5007T>C MANE Select	NP_940980.4:p.Val1669=