Canonical Allele Identifier: CA2618286430

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40363384-A-ATTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363393_40363394insTTTTTTTTTTTT , CM000674.2:g.40363393_40363394insTTTTTTTTTTTT	GRCh38
NC_000012.11:g.40757195_40757196insTTTTTTTTTTTT , CM000674.1:g.40757195_40757196insTTTTTTTTTTTT	GRCh37
NC_000012.10:g.39043462_39043463insTTTTTTTTTTTT	NCBI36
NG_011709.1:g.143383_143384insTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7029-9_7029-8insTTTTTTTTTTTT MANE Select	ENSP00000298910.7:n.7029-9_7029-8insTTTTTTTTTTTT
ENST00000636518.1:c.826-9_826-8insTTTTTTTTTTTT
ENST00000679360.1:c.*5938-9_*5938-8insTTTTTTTTTTTT	ENSP00000505368.1:n.*5938-9_*5938-8insTTTTTTTTTTTT
ENST00000679532.1:c.2803-9_2803-8insTTTTTTTTTTTT
ENST00000679683.1:c.819-9_819-8insTTTTTTTTTTTT
ENST00000680018.1:c.2474-9_2474-8insTTTTTTTTTTTT	ENSP00000505347.1:n.2474-9_2474-8insTTTTTTTTTTTT
ENST00000680422.1:c.4116-9_4116-8insTTTTTTTTTTTT
ENST00000680425.1:c.2196-9_2196-8insTTTTTTTTTTTT	ENSP00000506459.1:n.2196-9_2196-8insTTTTTTTTTTTT
ENST00000680453.1:c.2486-9_2486-8insTTTTTTTTTTTT
ENST00000680790.1:c.6774-9_6774-8insTTTTTTTTTTTT	ENSP00000505335.1:n.6774-9_6774-8insTTTTTTTTTTTT
ENST00000681136.1:n.3013-9_3013-8insTTTTTTTTTTTT
ENST00000681696.1:c.2712-9_2712-8insTTTTTTTTTTTT	ENSP00000505871.1:n.2712-9_2712-8insTTTTTTTTTTTT
ENST00000681773.1:n.236-9_236-8insTTTTTTTTTTTT
ENST00000298910.11:c.7029-9_7029-8insTTTTTTTTTTTT	ENSP00000298910.7:n.7029-9_7029-8insTTTTTTTTTTTT
ENST00000430804.5:c.4325-9_4325-8insTTTTTTTTTTTT
ENST00000479187.5:n.3710-9_3710-8insTTTTTTTTTTTT
NM_198578.3:c.7029-9_7029-8insTTTTTTTTTTTT	NP_940980.3:n.7029-9_7029-8insTTTTTTTTTTTT
XM_005268629.2:c.7029-9_7029-8insTTTTTTTTTTTT	XP_005268686.1:n.7029-9_7029-8insTTTTTTTTTTTT
XM_011537877.1:c.7029-9_7029-8insTTTTTTTTTTTT	XP_011536179.1:n.7029-9_7029-8insTTTTTTTTTTTT
XM_011537879.1:c.5826-9_5826-8insTTTTTTTTTTTT	XP_011536181.1:n.5826-9_5826-8insTTTTTTTTTTTT
XR_944868.1:n.485-8558_485-8557insAAAAAAAAAAAA
XM_005268629.4:c.7029-9_7029-8insTTTTTTTTTTTT	XP_005268686.1:n.7029-9_7029-8insTTTTTTTTTTTT
XM_011537877.3:c.7029-9_7029-8insTTTTTTTTTTTT	XP_011536179.1:n.7029-9_7029-8insTTTTTTTTTTTT
XM_017018787.1:c.3945-9_3945-8insTTTTTTTTTTTT	XP_016874276.1:n.3945-9_3945-8insTTTTTTTTTTTT
XM_017018788.2:c.3291-9_3291-8insTTTTTTTTTTTT	XP_016874277.1:n.3291-9_3291-8insTTTTTTTTTTTT
XM_024448833.1:c.5826-9_5826-8insTTTTTTTTTTTT	XP_024304601.1:n.5826-9_5826-8insTTTTTTTTTTTT
XR_944868.2:n.485-8558_485-8557insAAAAAAAAAAAA
NM_198578.4:c.7029-9_7029-8insTTTTTTTTTTTT MANE Select	NP_940980.4:n.7029-9_7029-8insTTTTTTTTTTTT