Canonical Allele Identifier: CA2031025257

Gene: LRRK2

Linked Data

• dbSNP Id: rs1946766723

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363183_40363184insCCAAAAGTAACCAA , CM000674.2:g.40363183_40363184insCCAAAAGTAACCAA	GRCh38
NC_000012.11:g.40756985_40756986insCCAAAAGTAACCAA , CM000674.1:g.40756985_40756986insCCAAAAGTAACCAA	GRCh37
NC_000012.10:g.39043252_39043253insCCAAAAGTAACCAA	NCBI36
NG_011709.1:g.143173_143174insCCAAAAGTAACCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7029-219_7029-218insCCAAAAGTAACCAA MANE Select	ENSP00000298910.7:n.7029-219_7029-218insCCAAAAGTAACCAA
ENST00000636518.1:c.826-219_826-218insCCAAAAGTAACCAA
ENST00000679360.1:c.*5938-219_*5938-218insCCAAAAGTAACCAA	ENSP00000505368.1:n.*5938-219_*5938-218insCCAAAAGTAACCAA
ENST00000679532.1:c.2803-219_2803-218insCCAAAAGTAACCAA
ENST00000679683.1:c.819-219_819-218insCCAAAAGTAACCAA
ENST00000680018.1:c.2474-219_2474-218insCCAAAAGTAACCAA	ENSP00000505347.1:n.2474-219_2474-218insCCAAAAGTAACCAA
ENST00000680422.1:c.4116-219_4116-218insCCAAAAGTAACCAA
ENST00000680425.1:c.2196-219_2196-218insCCAAAAGTAACCAA	ENSP00000506459.1:n.2196-219_2196-218insCCAAAAGTAACCAA
ENST00000680453.1:c.2486-219_2486-218insCCAAAAGTAACCAA
ENST00000680790.1:c.6774-219_6774-218insCCAAAAGTAACCAA	ENSP00000505335.1:n.6774-219_6774-218insCCAAAAGTAACCAA
ENST00000681136.1:n.3013-219_3013-218insCCAAAAGTAACCAA
ENST00000681696.1:c.2712-219_2712-218insCCAAAAGTAACCAA	ENSP00000505871.1:n.2712-219_2712-218insCCAAAAGTAACCAA
ENST00000681773.1:n.236-219_236-218insCCAAAAGTAACCAA
ENST00000298910.11:c.7029-219_7029-218insCCAAAAGTAACCAA	ENSP00000298910.7:n.7029-219_7029-218insCCAAAAGTAACCAA
ENST00000430804.5:c.4325-219_4325-218insCCAAAAGTAACCAA
ENST00000479187.5:n.3710-219_3710-218insCCAAAAGTAACCAA
NM_198578.3:c.7029-219_7029-218insCCAAAAGTAACCAA	NP_940980.3:n.7029-219_7029-218insCCAAAAGTAACCAA
XM_005268629.2:c.7029-219_7029-218insCCAAAAGTAACCAA	XP_005268686.1:n.7029-219_7029-218insCCAAAAGTAACCAA
XM_011537877.1:c.7029-219_7029-218insCCAAAAGTAACCAA	XP_011536179.1:n.7029-219_7029-218insCCAAAAGTAACCAA
XM_011537878.1:c.*658_*659insCCAAAAGTAACCAA	XP_011536180.1:n.*658_*659insCCAAAAGTAACCAA
XM_011537879.1:c.5826-219_5826-218insCCAAAAGTAACCAA	XP_011536181.1:n.5826-219_5826-218insCCAAAAGTAACCAA
XR_944868.1:n.485-8355_485-8354insGGTTACTTTTGGTT
XM_005268629.4:c.7029-219_7029-218insCCAAAAGTAACCAA	XP_005268686.1:n.7029-219_7029-218insCCAAAAGTAACCAA
XM_011537877.3:c.7029-219_7029-218insCCAAAAGTAACCAA	XP_011536179.1:n.7029-219_7029-218insCCAAAAGTAACCAA
XM_017018787.1:c.3945-219_3945-218insCCAAAAGTAACCAA	XP_016874276.1:n.3945-219_3945-218insCCAAAAGTAACCAA
XM_017018788.2:c.3291-219_3291-218insCCAAAAGTAACCAA	XP_016874277.1:n.3291-219_3291-218insCCAAAAGTAACCAA
XM_024448833.1:c.5826-219_5826-218insCCAAAAGTAACCAA	XP_024304601.1:n.5826-219_5826-218insCCAAAAGTAACCAA
XR_944868.2:n.485-8355_485-8354insGGTTACTTTTGGTT
NM_198578.4:c.7029-219_7029-218insCCAAAAGTAACCAA MANE Select	NP_940980.4:n.7029-219_7029-218insCCAAAAGTAACCAA