Canonical Allele Identifier: CA479238659

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734186A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340384A>C , CM000674.2:g.40340384A>C	GRCh38
NC_000012.11:g.40734186A>C , CM000674.1:g.40734186A>C	GRCh37
NC_000012.10:g.39020453A>C	NCBI36
NG_011709.1:g.120374A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6039A>C MANE Select	ENSP00000298910.7:p.Ala2013=
ENST00000679360.1:c.*4948A>C	ENSP00000505368.1:n.*4948A>C
ENST00000679532.1:c.1813A>C
ENST00000680018.1:c.1484A>C	ENSP00000505347.1:n.1484A>C
ENST00000680422.1:c.1684A>C
ENST00000680425.1:c.1206A>C	ENSP00000506459.1:n.1206A>C
ENST00000680453.1:c.1496A>C
ENST00000680790.1:c.5784A>C	ENSP00000505335.1:p.Ala1928=
ENST00000681136.1:n.2023A>C
ENST00000681696.1:c.1722A>C	ENSP00000505871.1:p.Ala574=
ENST00000298910.11:c.6039A>C	ENSP00000298910.7:p.Ala2013=
ENST00000430804.5:c.3335A>C
ENST00000479187.5:n.2720A>C
NM_198578.3:c.6039A>C	NP_940980.3:p.Ala2013=
XM_005268629.2:c.6039A>C	XP_005268686.1:p.Ala2013=
XM_011537877.1:c.6039A>C	XP_011536179.1:p.Ala2013=
XM_011537878.1:c.6039A>C	XP_011536180.1:p.Ala2013=
XM_011537879.1:c.4836A>C	XP_011536181.1:p.Ala1612=
XM_005268629.4:c.6039A>C	XP_005268686.1:p.Ala2013=
XM_011537877.3:c.6039A>C	XP_011536179.1:p.Ala2013=
XM_017018787.1:c.2955A>C	XP_016874276.1:p.Ala985=
XM_017018788.2:c.2301A>C	XP_016874277.1:p.Ala767=
XM_024448833.1:c.4836A>C	XP_024304601.1:p.Ala1612=
NM_198578.4:c.6039A>C MANE Select	NP_940980.4:p.Ala2013=