Canonical Allele Identifier: CA384421178

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40717069G>C (hg19) ; chr12:g.40323267G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40323267G>C , CM000674.2:g.40323267G>C	GRCh38
NC_000012.11:g.40717069G>C , CM000674.1:g.40717069G>C	GRCh37
NC_000012.10:g.39003336G>C	NCBI36
NG_011709.1:g.103257G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5617G>C MANE Select	ENSP00000298910.7:p.Asp1873His
ENST00000679360.1:c.*4526G>C	ENSP00000505368.1:n.*4526G>C
ENST00000679532.1:c.1391G>C
ENST00000680018.1:c.1062G>C	ENSP00000505347.1:n.1062G>C
ENST00000680422.1:c.1262G>C
ENST00000680425.1:c.784G>C	ENSP00000506459.1:n.784G>C
ENST00000680453.1:c.1074G>C
ENST00000680790.1:c.5362G>C	ENSP00000505335.1:p.Asp1788His
ENST00000681136.1:n.1601G>C
ENST00000681696.1:c.1300G>C	ENSP00000505871.1:p.Asp434His
ENST00000298910.11:c.5617G>C	ENSP00000298910.7:p.Asp1873His
ENST00000430804.5:c.2913G>C
ENST00000479187.5:n.2298G>C
NM_198578.3:c.5617G>C	NP_940980.3:p.Asp1873His
XM_005268629.2:c.5617G>C	XP_005268686.1:p.Asp1873His
XM_011537877.1:c.5617G>C	XP_011536179.1:p.Asp1873His
XM_011537878.1:c.5617G>C	XP_011536180.1:p.Asp1873His
XM_011537879.1:c.4414G>C	XP_011536181.1:p.Asp1472His
XM_005268629.4:c.5617G>C	XP_005268686.1:p.Asp1873His
XM_011537877.3:c.5617G>C	XP_011536179.1:p.Asp1873His
XM_017018787.1:c.2533G>C	XP_016874276.1:p.Asp845His
XM_017018788.2:c.1879G>C	XP_016874277.1:p.Asp627His
XM_024448833.1:c.4414G>C	XP_024304601.1:p.Asp1472His
NM_198578.4:c.5617G>C MANE Select	NP_940980.4:p.Asp1873His