Canonical Allele Identifier: CA384404086

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734226A>C (hg19) ; chr12:g.40340424A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340424A>C , CM000674.2:g.40340424A>C	GRCh38
NC_000012.11:g.40734226A>C , CM000674.1:g.40734226A>C	GRCh37
NC_000012.10:g.39020493A>C	NCBI36
NG_011709.1:g.120414A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.6079A>C MANE Select	ENSP00000298910.7:p.Met2027Leu
ENST00000679360.1:c.*4988A>C	ENSP00000505368.1:n.*4988A>C
ENST00000679532.1:c.1853A>C
ENST00000680018.1:c.1524A>C	ENSP00000505347.1:n.1524A>C
ENST00000680422.1:c.1724A>C
ENST00000680425.1:c.1246A>C	ENSP00000506459.1:n.1246A>C
ENST00000680453.1:c.1536A>C
ENST00000680790.1:c.5824A>C	ENSP00000505335.1:p.Met1942Leu
ENST00000681136.1:n.2063A>C
ENST00000681696.1:c.1762A>C	ENSP00000505871.1:p.Met588Leu
ENST00000298910.11:c.6079A>C	ENSP00000298910.7:p.Met2027Leu
ENST00000430804.5:c.3375A>C
ENST00000479187.5:n.2760A>C
NM_198578.3:c.6079A>C	NP_940980.3:p.Met2027Leu
XM_005268629.2:c.6079A>C	XP_005268686.1:p.Met2027Leu
XM_011537877.1:c.6079A>C	XP_011536179.1:p.Met2027Leu
XM_011537878.1:c.6079A>C	XP_011536180.1:p.Met2027Leu
XM_011537879.1:c.4876A>C	XP_011536181.1:p.Met1626Leu
XM_005268629.4:c.6079A>C	XP_005268686.1:p.Met2027Leu
XM_011537877.3:c.6079A>C	XP_011536179.1:p.Met2027Leu
XM_017018787.1:c.2995A>C	XP_016874276.1:p.Met999Leu
XM_017018788.2:c.2341A>C	XP_016874277.1:p.Met781Leu
XM_024448833.1:c.4876A>C	XP_024304601.1:p.Met1626Leu
NM_198578.4:c.6079A>C MANE Select	NP_940980.4:p.Met2027Leu