Canonical Allele Identifier: CA384420978

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40716977A>C (hg19) ; chr12:g.40323175A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40323175A>C , CM000674.2:g.40323175A>C	GRCh38
NC_000012.11:g.40716977A>C , CM000674.1:g.40716977A>C	GRCh37
NC_000012.10:g.39003244A>C	NCBI36
NG_011709.1:g.103165A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5525A>C MANE Select	ENSP00000298910.7:p.Asn1842Thr
ENST00000679360.1:c.*4434A>C	ENSP00000505368.1:n.*4434A>C
ENST00000679532.1:c.1299A>C
ENST00000680018.1:c.970A>C	ENSP00000505347.1:n.970A>C
ENST00000680422.1:c.1170A>C
ENST00000680425.1:c.692A>C	ENSP00000506459.1:n.692A>C
ENST00000680453.1:c.982A>C
ENST00000680790.1:c.5270A>C	ENSP00000505335.1:p.Asn1757Thr
ENST00000681136.1:n.1509A>C
ENST00000681696.1:c.1208A>C	ENSP00000505871.1:p.Asn403Thr
ENST00000298910.11:c.5525A>C	ENSP00000298910.7:p.Asn1842Thr
ENST00000430804.5:c.2821A>C
ENST00000479187.5:n.2206A>C
NM_198578.3:c.5525A>C	NP_940980.3:p.Asn1842Thr
XM_005268629.2:c.5525A>C	XP_005268686.1:p.Asn1842Thr
XM_011537877.1:c.5525A>C	XP_011536179.1:p.Asn1842Thr
XM_011537878.1:c.5525A>C	XP_011536180.1:p.Asn1842Thr
XM_011537879.1:c.4322A>C	XP_011536181.1:p.Asn1441Thr
XM_005268629.4:c.5525A>C	XP_005268686.1:p.Asn1842Thr
XM_011537877.3:c.5525A>C	XP_011536179.1:p.Asn1842Thr
XM_017018787.1:c.2441A>C	XP_016874276.1:p.Asn814Thr
XM_017018788.2:c.1787A>C	XP_016874277.1:p.Asn596Thr
XM_024448833.1:c.4322A>C	XP_024304601.1:p.Asn1441Thr
NM_198578.4:c.5525A>C MANE Select	NP_940980.4:p.Asn1842Thr