Canonical Allele Identifier: CA479238810

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734231G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340429G>C , CM000674.2:g.40340429G>C	GRCh38
NC_000012.11:g.40734231G>C , CM000674.1:g.40734231G>C	GRCh37
NC_000012.10:g.39020498G>C	NCBI36
NG_011709.1:g.120419G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6084G>C MANE Select	ENSP00000298910.7:p.Gly2028=
ENST00000679360.1:c.*4993G>C	ENSP00000505368.1:n.*4993G>C
ENST00000679532.1:c.1858G>C
ENST00000680018.1:c.1529G>C	ENSP00000505347.1:n.1529G>C
ENST00000680422.1:c.1729G>C
ENST00000680425.1:c.1251G>C	ENSP00000506459.1:n.1251G>C
ENST00000680453.1:c.1541G>C
ENST00000680790.1:c.5829G>C	ENSP00000505335.1:p.Gly1943=
ENST00000681136.1:n.2068G>C
ENST00000681696.1:c.1767G>C	ENSP00000505871.1:p.Gly589=
ENST00000298910.11:c.6084G>C	ENSP00000298910.7:p.Gly2028=
ENST00000430804.5:c.3380G>C
ENST00000479187.5:n.2765G>C
NM_198578.3:c.6084G>C	NP_940980.3:p.Gly2028=
XM_005268629.2:c.6084G>C	XP_005268686.1:p.Gly2028=
XM_011537877.1:c.6084G>C	XP_011536179.1:p.Gly2028=
XM_011537878.1:c.6084G>C	XP_011536180.1:p.Gly2028=
XM_011537879.1:c.4881G>C	XP_011536181.1:p.Gly1627=
XM_005268629.4:c.6084G>C	XP_005268686.1:p.Gly2028=
XM_011537877.3:c.6084G>C	XP_011536179.1:p.Gly2028=
XM_017018787.1:c.3000G>C	XP_016874276.1:p.Gly1000=
XM_017018788.2:c.2346G>C	XP_016874277.1:p.Gly782=
XM_024448833.1:c.4881G>C	XP_024304601.1:p.Gly1627=
NM_198578.4:c.6084G>C MANE Select	NP_940980.4:p.Gly2028=