Canonical Allele Identifier: CA384421181

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40717070A>T (hg19) ; chr12:g.40323268A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40323268A>T , CM000674.2:g.40323268A>T	GRCh38
NC_000012.11:g.40717070A>T , CM000674.1:g.40717070A>T	GRCh37
NC_000012.10:g.39003337A>T	NCBI36
NG_011709.1:g.103258A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5618A>T MANE Select	ENSP00000298910.7:p.Asp1873Val
ENST00000679360.1:c.*4527A>T	ENSP00000505368.1:n.*4527A>T
ENST00000679532.1:c.1392A>T
ENST00000680018.1:c.1063A>T	ENSP00000505347.1:n.1063A>T
ENST00000680422.1:c.1263A>T
ENST00000680425.1:c.785A>T	ENSP00000506459.1:n.785A>T
ENST00000680453.1:c.1075A>T
ENST00000680790.1:c.5363A>T	ENSP00000505335.1:p.Asp1788Val
ENST00000681136.1:n.1602A>T
ENST00000681696.1:c.1301A>T	ENSP00000505871.1:p.Asp434Val
ENST00000298910.11:c.5618A>T	ENSP00000298910.7:p.Asp1873Val
ENST00000430804.5:c.2914A>T
ENST00000479187.5:n.2299A>T
NM_198578.3:c.5618A>T	NP_940980.3:p.Asp1873Val
XM_005268629.2:c.5618A>T	XP_005268686.1:p.Asp1873Val
XM_011537877.1:c.5618A>T	XP_011536179.1:p.Asp1873Val
XM_011537878.1:c.5618A>T	XP_011536180.1:p.Asp1873Val
XM_011537879.1:c.4415A>T	XP_011536181.1:p.Asp1472Val
XM_005268629.4:c.5618A>T	XP_005268686.1:p.Asp1873Val
XM_011537877.3:c.5618A>T	XP_011536179.1:p.Asp1873Val
XM_017018787.1:c.2534A>T	XP_016874276.1:p.Asp845Val
XM_017018788.2:c.1880A>T	XP_016874277.1:p.Asp627Val
XM_024448833.1:c.4415A>T	XP_024304601.1:p.Asp1472Val
NM_198578.4:c.5618A>T MANE Select	NP_940980.4:p.Asp1873Val