Canonical Allele Identifier: CA384420982

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40716979C>A (hg19) ; chr12:g.40323177C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40323177C>A , CM000674.2:g.40323177C>A	GRCh38
NC_000012.11:g.40716979C>A , CM000674.1:g.40716979C>A	GRCh37
NC_000012.10:g.39003246C>A	NCBI36
NG_011709.1:g.103167C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5527C>A MANE Select	ENSP00000298910.7:p.Pro1843Thr
ENST00000679360.1:c.*4436C>A	ENSP00000505368.1:n.*4436C>A
ENST00000679532.1:c.1301C>A
ENST00000680018.1:c.972C>A	ENSP00000505347.1:n.972C>A
ENST00000680422.1:c.1172C>A
ENST00000680425.1:c.694C>A	ENSP00000506459.1:n.694C>A
ENST00000680453.1:c.984C>A
ENST00000680790.1:c.5272C>A	ENSP00000505335.1:p.Pro1758Thr
ENST00000681136.1:n.1511C>A
ENST00000681696.1:c.1210C>A	ENSP00000505871.1:p.Pro404Thr
ENST00000298910.11:c.5527C>A	ENSP00000298910.7:p.Pro1843Thr
ENST00000430804.5:c.2823C>A
ENST00000479187.5:n.2208C>A
NM_198578.3:c.5527C>A	NP_940980.3:p.Pro1843Thr
XM_005268629.2:c.5527C>A	XP_005268686.1:p.Pro1843Thr
XM_011537877.1:c.5527C>A	XP_011536179.1:p.Pro1843Thr
XM_011537878.1:c.5527C>A	XP_011536180.1:p.Pro1843Thr
XM_011537879.1:c.4324C>A	XP_011536181.1:p.Pro1442Thr
XM_005268629.4:c.5527C>A	XP_005268686.1:p.Pro1843Thr
XM_011537877.3:c.5527C>A	XP_011536179.1:p.Pro1843Thr
XM_017018787.1:c.2443C>A	XP_016874276.1:p.Pro815Thr
XM_017018788.2:c.1789C>A	XP_016874277.1:p.Pro597Thr
XM_024448833.1:c.4324C>A	XP_024304601.1:p.Pro1442Thr
NM_198578.4:c.5527C>A MANE Select	NP_940980.4:p.Pro1843Thr