Canonical Allele Identifier: CA479238520

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734150G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340348G>T , CM000674.2:g.40340348G>T	GRCh38
NC_000012.11:g.40734150G>T , CM000674.1:g.40734150G>T	GRCh37
NC_000012.10:g.39020417G>T	NCBI36
NG_011709.1:g.120338G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6003G>T MANE Select	ENSP00000298910.7:p.Leu2001=
ENST00000679360.1:c.*4912G>T	ENSP00000505368.1:n.*4912G>T
ENST00000679532.1:c.1777G>T
ENST00000680018.1:c.1448G>T	ENSP00000505347.1:n.1448G>T
ENST00000680422.1:c.1648G>T
ENST00000680425.1:c.1170G>T	ENSP00000506459.1:n.1170G>T
ENST00000680453.1:c.1460G>T
ENST00000680790.1:c.5748G>T	ENSP00000505335.1:p.Leu1916=
ENST00000681136.1:n.1987G>T
ENST00000681696.1:c.1686G>T	ENSP00000505871.1:p.Leu562=
ENST00000298910.11:c.6003G>T	ENSP00000298910.7:p.Leu2001=
ENST00000430804.5:c.3299G>T
ENST00000479187.5:n.2684G>T
NM_198578.3:c.6003G>T	NP_940980.3:p.Leu2001=
XM_005268629.2:c.6003G>T	XP_005268686.1:p.Leu2001=
XM_011537877.1:c.6003G>T	XP_011536179.1:p.Leu2001=
XM_011537878.1:c.6003G>T	XP_011536180.1:p.Leu2001=
XM_011537879.1:c.4800G>T	XP_011536181.1:p.Leu1600=
XM_005268629.4:c.6003G>T	XP_005268686.1:p.Leu2001=
XM_011537877.3:c.6003G>T	XP_011536179.1:p.Leu2001=
XM_017018787.1:c.2919G>T	XP_016874276.1:p.Leu973=
XM_017018788.2:c.2265G>T	XP_016874277.1:p.Leu755=
XM_024448833.1:c.4800G>T	XP_024304601.1:p.Leu1600=
NM_198578.4:c.6003G>T MANE Select	NP_940980.4:p.Leu2001=