Canonical Allele Identifier: CA2031025418

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363266_40363267delinsAT , CM000674.2:g.40363266_40363267delinsAT	GRCh38
NC_000012.11:g.40757068_40757069delinsAT , CM000674.1:g.40757068_40757069delinsAT	GRCh37
NC_000012.10:g.39043335_39043336delinsAT	NCBI36
NG_011709.1:g.143256_143257delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7029-136_7029-135delinsAT MANE Select	ENSP00000298910.7:n.7029-136_7029-135delinsAT
ENST00000636518.1:c.826-136_826-135delinsAT
ENST00000679360.1:c.*5938-136_*5938-135delinsAT	ENSP00000505368.1:n.*5938-136_*5938-135delinsAT
ENST00000679532.1:c.2803-136_2803-135delinsAT
ENST00000679683.1:c.819-136_819-135delinsAT
ENST00000680018.1:c.2474-136_2474-135delinsAT	ENSP00000505347.1:n.2474-136_2474-135delinsAT
ENST00000680422.1:c.4116-136_4116-135delinsAT
ENST00000680425.1:c.2196-136_2196-135delinsAT	ENSP00000506459.1:n.2196-136_2196-135delinsAT
ENST00000680453.1:c.2486-136_2486-135delinsAT
ENST00000680790.1:c.6774-136_6774-135delinsAT	ENSP00000505335.1:n.6774-136_6774-135delinsAT
ENST00000681136.1:n.3013-136_3013-135delinsAT
ENST00000681696.1:c.2712-136_2712-135delinsAT	ENSP00000505871.1:n.2712-136_2712-135delinsAT
ENST00000681773.1:n.236-136_236-135delinsAT
ENST00000298910.11:c.7029-136_7029-135delinsAT	ENSP00000298910.7:n.7029-136_7029-135delinsAT
ENST00000430804.5:c.4325-136_4325-135delinsAT
ENST00000479187.5:n.3710-136_3710-135delinsAT
NM_198578.3:c.7029-136_7029-135delinsAT	NP_940980.3:n.7029-136_7029-135delinsAT
XM_005268629.2:c.7029-136_7029-135delinsAT	XP_005268686.1:n.7029-136_7029-135delinsAT
XM_011537877.1:c.7029-136_7029-135delinsAT	XP_011536179.1:n.7029-136_7029-135delinsAT
XM_011537878.1:c.*741_*742delinsAT	XP_011536180.1:n.*741_*742delinsAT
XM_011537879.1:c.5826-136_5826-135delinsAT	XP_011536181.1:n.5826-136_5826-135delinsAT
XR_944868.1:n.485-8440_485-8439delinsAT
XM_005268629.4:c.7029-136_7029-135delinsAT	XP_005268686.1:n.7029-136_7029-135delinsAT
XM_011537877.3:c.7029-136_7029-135delinsAT	XP_011536179.1:n.7029-136_7029-135delinsAT
XM_017018787.1:c.3945-136_3945-135delinsAT	XP_016874276.1:n.3945-136_3945-135delinsAT
XM_017018788.2:c.3291-136_3291-135delinsAT	XP_016874277.1:n.3291-136_3291-135delinsAT
XM_024448833.1:c.5826-136_5826-135delinsAT	XP_024304601.1:n.5826-136_5826-135delinsAT
XR_944868.2:n.485-8440_485-8439delinsAT
NM_198578.4:c.7029-136_7029-135delinsAT MANE Select	NP_940980.4:n.7029-136_7029-135delinsAT