Canonical Allele Identifier: CA2031027093

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340281C= , CM000674.2:g.40340281C=	GRCh38
NC_000012.11:g.40734083C= , CM000674.1:g.40734083C=	GRCh37
NC_000012.10:g.39020350C=	NCBI36
NG_011709.1:g.120271C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5949-13C= MANE Select	ENSP00000298910.7:n.5949-13C=
ENST00000679360.1:c.*4858-13C=	ENSP00000505368.1:n.*4858-13C=
ENST00000679532.1:c.1723-13C=
ENST00000680018.1:c.1394-13C=	ENSP00000505347.1:n.1394-13C=
ENST00000680422.1:c.1594-13C=
ENST00000680425.1:c.1116-13C=	ENSP00000506459.1:n.1116-13C=
ENST00000680453.1:c.1406-13C=
ENST00000680790.1:c.5694-13C=	ENSP00000505335.1:n.5694-13C=
ENST00000681136.1:n.1933-13C=
ENST00000681696.1:c.1632-13C=	ENSP00000505871.1:n.1632-13C=
ENST00000298910.11:c.5949-13C=	ENSP00000298910.7:n.5949-13C=
ENST00000430804.5:c.3245-13C=
ENST00000479187.5:n.2630-13C=
NM_198578.3:c.5949-13C=	NP_940980.3:n.5949-13C=
XM_005268629.2:c.5949-13C=	XP_005268686.1:n.5949-13C=
XM_011537877.1:c.5949-13C=	XP_011536179.1:n.5949-13C=
XM_011537878.1:c.5949-13C=	XP_011536180.1:n.5949-13C=
XM_011537879.1:c.4746-13C=	XP_011536181.1:n.4746-13C=
XM_005268629.4:c.5949-13C=	XP_005268686.1:n.5949-13C=
XM_011537877.3:c.5949-13C=	XP_011536179.1:n.5949-13C=
XM_017018787.1:c.2865-13C=	XP_016874276.1:n.2865-13C=
XM_017018788.2:c.2211-13C=	XP_016874277.1:n.2211-13C=
XM_024448833.1:c.4746-13C=	XP_024304601.1:n.4746-13C=
NM_198578.4:c.5949-13C= MANE Select	NP_940980.4:n.5949-13C=