Canonical Allele Identifier: CA2532943883

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363295_40363296insCAATTCTATG , CM000674.2:g.40363295_40363296insCAATTCTATG	GRCh38
NC_000012.11:g.40757097_40757098insCAATTCTATG , CM000674.1:g.40757097_40757098insCAATTCTATG	GRCh37
NC_000012.10:g.39043364_39043365insCAATTCTATG	NCBI36
NG_011709.1:g.143285_143286insCAATTCTATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7029-107_7029-106insCAATTCTATG MANE Select	ENSP00000298910.7:n.7029-107_7029-106insCAATTCTATG
ENST00000636518.1:c.826-107_826-106insCAATTCTATG
ENST00000679360.1:c.*5938-107_*5938-106insCAATTCTATG	ENSP00000505368.1:n.*5938-107_*5938-106insCAATTCTATG
ENST00000679532.1:c.2803-107_2803-106insCAATTCTATG
ENST00000679683.1:c.819-107_819-106insCAATTCTATG
ENST00000680018.1:c.2474-107_2474-106insCAATTCTATG	ENSP00000505347.1:n.2474-107_2474-106insCAATTCTATG
ENST00000680422.1:c.4116-107_4116-106insCAATTCTATG
ENST00000680425.1:c.2196-107_2196-106insCAATTCTATG	ENSP00000506459.1:n.2196-107_2196-106insCAATTCTATG
ENST00000680453.1:c.2486-107_2486-106insCAATTCTATG
ENST00000680790.1:c.6774-107_6774-106insCAATTCTATG	ENSP00000505335.1:n.6774-107_6774-106insCAATTCTATG
ENST00000681136.1:n.3013-107_3013-106insCAATTCTATG
ENST00000681696.1:c.2712-107_2712-106insCAATTCTATG	ENSP00000505871.1:n.2712-107_2712-106insCAATTCTATG
ENST00000681773.1:n.236-107_236-106insCAATTCTATG
ENST00000298910.11:c.7029-107_7029-106insCAATTCTATG	ENSP00000298910.7:n.7029-107_7029-106insCAATTCTATG
ENST00000430804.5:c.4325-107_4325-106insCAATTCTATG
ENST00000479187.5:n.3710-107_3710-106insCAATTCTATG
NM_198578.3:c.7029-107_7029-106insCAATTCTATG	NP_940980.3:n.7029-107_7029-106insCAATTCTATG
XM_005268629.2:c.7029-107_7029-106insCAATTCTATG	XP_005268686.1:n.7029-107_7029-106insCAATTCTATG
XM_011537877.1:c.7029-107_7029-106insCAATTCTATG	XP_011536179.1:n.7029-107_7029-106insCAATTCTATG
XM_011537878.1:c.*770_*771insCAATTCTATG	XP_011536180.1:n.*770_*771insCAATTCTATG
XM_011537879.1:c.5826-107_5826-106insCAATTCTATG	XP_011536181.1:n.5826-107_5826-106insCAATTCTATG
XR_944868.1:n.485-8469_485-8468insCATAGAATTG
XM_005268629.4:c.7029-107_7029-106insCAATTCTATG	XP_005268686.1:n.7029-107_7029-106insCAATTCTATG
XM_011537877.3:c.7029-107_7029-106insCAATTCTATG	XP_011536179.1:n.7029-107_7029-106insCAATTCTATG
XM_017018787.1:c.3945-107_3945-106insCAATTCTATG	XP_016874276.1:n.3945-107_3945-106insCAATTCTATG
XM_017018788.2:c.3291-107_3291-106insCAATTCTATG	XP_016874277.1:n.3291-107_3291-106insCAATTCTATG
XM_024448833.1:c.5826-107_5826-106insCAATTCTATG	XP_024304601.1:n.5826-107_5826-106insCAATTCTATG
XR_944868.2:n.485-8469_485-8468insCATAGAATTG
NM_198578.4:c.7029-107_7029-106insCAATTCTATG MANE Select	NP_940980.4:n.7029-107_7029-106insCAATTCTATG