Canonical Allele Identifier: CA384403595

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734127G>C (hg19) ; chr12:g.40340325G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340325G>C , CM000674.2:g.40340325G>C	GRCh38
NC_000012.11:g.40734127G>C , CM000674.1:g.40734127G>C	GRCh37
NC_000012.10:g.39020394G>C	NCBI36
NG_011709.1:g.120315G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5980G>C MANE Select	ENSP00000298910.7:p.Asp1994His
ENST00000679360.1:c.*4889G>C	ENSP00000505368.1:n.*4889G>C
ENST00000679532.1:c.1754G>C
ENST00000680018.1:c.1425G>C	ENSP00000505347.1:n.1425G>C
ENST00000680422.1:c.1625G>C
ENST00000680425.1:c.1147G>C	ENSP00000506459.1:n.1147G>C
ENST00000680453.1:c.1437G>C
ENST00000680790.1:c.5725G>C	ENSP00000505335.1:p.Asp1909His
ENST00000681136.1:n.1964G>C
ENST00000681696.1:c.1663G>C	ENSP00000505871.1:p.Asp555His
ENST00000298910.11:c.5980G>C	ENSP00000298910.7:p.Asp1994His
ENST00000430804.5:c.3276G>C
ENST00000479187.5:n.2661G>C
NM_198578.3:c.5980G>C	NP_940980.3:p.Asp1994His
XM_005268629.2:c.5980G>C	XP_005268686.1:p.Asp1994His
XM_011537877.1:c.5980G>C	XP_011536179.1:p.Asp1994His
XM_011537878.1:c.5980G>C	XP_011536180.1:p.Asp1994His
XM_011537879.1:c.4777G>C	XP_011536181.1:p.Asp1593His
XM_005268629.4:c.5980G>C	XP_005268686.1:p.Asp1994His
XM_011537877.3:c.5980G>C	XP_011536179.1:p.Asp1994His
XM_017018787.1:c.2896G>C	XP_016874276.1:p.Asp966His
XM_017018788.2:c.2242G>C	XP_016874277.1:p.Asp748His
XM_024448833.1:c.4777G>C	XP_024304601.1:p.Asp1593His
NM_198578.4:c.5980G>C MANE Select	NP_940980.4:p.Asp1994His