Canonical Allele Identifier: CA2031027490

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340532_40340533delinsCA , CM000674.2:g.40340532_40340533delinsCA	GRCh38
NC_000012.11:g.40734334_40734335delinsCA , CM000674.1:g.40734334_40734335delinsCA	GRCh37
NC_000012.10:g.39020601_39020602delinsCA	NCBI36
NG_011709.1:g.120522_120523delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6109+78_6109+79delinsCA MANE Select	ENSP00000298910.7:n.6109+78_6109+79delinsCA
ENST00000679360.1:c.*5018+78_*5018+79delinsCA	ENSP00000505368.1:n.*5018+78_*5018+79delinsCA
ENST00000679532.1:c.1883+78_1883+79delinsCA
ENST00000680018.1:c.1554+78_1554+79delinsCA	ENSP00000505347.1:n.1554+78_1554+79delinsCA
ENST00000680422.1:c.1754+78_1754+79delinsCA
ENST00000680425.1:c.1276+78_1276+79delinsCA	ENSP00000506459.1:n.1276+78_1276+79delinsCA
ENST00000680453.1:c.1566+78_1566+79delinsCA
ENST00000680790.1:c.5854+78_5854+79delinsCA	ENSP00000505335.1:n.5854+78_5854+79delinsCA
ENST00000681136.1:n.2093+78_2093+79delinsCA
ENST00000681696.1:c.1792+78_1792+79delinsCA	ENSP00000505871.1:n.1792+78_1792+79delinsCA
ENST00000298910.11:c.6109+78_6109+79delinsCA	ENSP00000298910.7:n.6109+78_6109+79delinsCA
ENST00000430804.5:c.3405+78_3405+79delinsCA
ENST00000479187.5:n.2790+78_2790+79delinsCA
NM_198578.3:c.6109+78_6109+79delinsCA	NP_940980.3:n.6109+78_6109+79delinsCA
XM_005268629.2:c.6109+78_6109+79delinsCA	XP_005268686.1:n.6109+78_6109+79delinsCA
XM_011537877.1:c.6109+78_6109+79delinsCA	XP_011536179.1:n.6109+78_6109+79delinsCA
XM_011537878.1:c.6109+78_6109+79delinsCA	XP_011536180.1:n.6109+78_6109+79delinsCA
XM_011537879.1:c.4906+78_4906+79delinsCA	XP_011536181.1:n.4906+78_4906+79delinsCA
XM_005268629.4:c.6109+78_6109+79delinsCA	XP_005268686.1:n.6109+78_6109+79delinsCA
XM_011537877.3:c.6109+78_6109+79delinsCA	XP_011536179.1:n.6109+78_6109+79delinsCA
XM_017018787.1:c.3025+78_3025+79delinsCA	XP_016874276.1:n.3025+78_3025+79delinsCA
XM_017018788.2:c.2371+78_2371+79delinsCA	XP_016874277.1:n.2371+78_2371+79delinsCA
XM_024448833.1:c.4906+78_4906+79delinsCA	XP_024304601.1:n.4906+78_4906+79delinsCA
NM_198578.4:c.6109+78_6109+79delinsCA MANE Select	NP_940980.4:n.6109+78_6109+79delinsCA