Canonical Allele Identifier: CA479238458

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734132G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340330G>C , CM000674.2:g.40340330G>C	GRCh38
NC_000012.11:g.40734132G>C , CM000674.1:g.40734132G>C	GRCh37
NC_000012.10:g.39020399G>C	NCBI36
NG_011709.1:g.120320G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5985G>C MANE Select	ENSP00000298910.7:p.Leu1995=
ENST00000679360.1:c.*4894G>C	ENSP00000505368.1:n.*4894G>C
ENST00000679532.1:c.1759G>C
ENST00000680018.1:c.1430G>C	ENSP00000505347.1:n.1430G>C
ENST00000680422.1:c.1630G>C
ENST00000680425.1:c.1152G>C	ENSP00000506459.1:n.1152G>C
ENST00000680453.1:c.1442G>C
ENST00000680790.1:c.5730G>C	ENSP00000505335.1:p.Leu1910=
ENST00000681136.1:n.1969G>C
ENST00000681696.1:c.1668G>C	ENSP00000505871.1:p.Leu556=
ENST00000298910.11:c.5985G>C	ENSP00000298910.7:p.Leu1995=
ENST00000430804.5:c.3281G>C
ENST00000479187.5:n.2666G>C
NM_198578.3:c.5985G>C	NP_940980.3:p.Leu1995=
XM_005268629.2:c.5985G>C	XP_005268686.1:p.Leu1995=
XM_011537877.1:c.5985G>C	XP_011536179.1:p.Leu1995=
XM_011537878.1:c.5985G>C	XP_011536180.1:p.Leu1995=
XM_011537879.1:c.4782G>C	XP_011536181.1:p.Leu1594=
XM_005268629.4:c.5985G>C	XP_005268686.1:p.Leu1995=
XM_011537877.3:c.5985G>C	XP_011536179.1:p.Leu1995=
XM_017018787.1:c.2901G>C	XP_016874276.1:p.Leu967=
XM_017018788.2:c.2247G>C	XP_016874277.1:p.Leu749=
XM_024448833.1:c.4782G>C	XP_024304601.1:p.Leu1594=
NM_198578.4:c.5985G>C MANE Select	NP_940980.4:p.Leu1995=