Canonical Allele Identifier: CA2618286378

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40363311-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363311_40363312insTC , CM000674.2:g.40363311_40363312insTC	GRCh38
NC_000012.11:g.40757113_40757114insTC , CM000674.1:g.40757113_40757114insTC	GRCh37
NC_000012.10:g.39043380_39043381insTC	NCBI36
NG_011709.1:g.143301_143302insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7029-91_7029-90insTC MANE Select	ENSP00000298910.7:n.7029-91_7029-90insTC
ENST00000636518.1:c.826-91_826-90insTC
ENST00000679360.1:c.*5938-91_*5938-90insTC	ENSP00000505368.1:n.*5938-91_*5938-90insTC
ENST00000679532.1:c.2803-91_2803-90insTC
ENST00000679683.1:c.819-91_819-90insTC
ENST00000680018.1:c.2474-91_2474-90insTC	ENSP00000505347.1:n.2474-91_2474-90insTC
ENST00000680422.1:c.4116-91_4116-90insTC
ENST00000680425.1:c.2196-91_2196-90insTC	ENSP00000506459.1:n.2196-91_2196-90insTC
ENST00000680453.1:c.2486-91_2486-90insTC
ENST00000680790.1:c.6774-91_6774-90insTC	ENSP00000505335.1:n.6774-91_6774-90insTC
ENST00000681136.1:n.3013-91_3013-90insTC
ENST00000681696.1:c.2712-91_2712-90insTC	ENSP00000505871.1:n.2712-91_2712-90insTC
ENST00000681773.1:n.236-91_236-90insTC
ENST00000298910.11:c.7029-91_7029-90insTC	ENSP00000298910.7:n.7029-91_7029-90insTC
ENST00000430804.5:c.4325-91_4325-90insTC
ENST00000479187.5:n.3710-91_3710-90insTC
NM_198578.3:c.7029-91_7029-90insTC	NP_940980.3:n.7029-91_7029-90insTC
XM_005268629.2:c.7029-91_7029-90insTC	XP_005268686.1:n.7029-91_7029-90insTC
XM_011537877.1:c.7029-91_7029-90insTC	XP_011536179.1:n.7029-91_7029-90insTC
XM_011537878.1:c.*786_*787insTC	XP_011536180.1:n.*786_*787insTC
XM_011537879.1:c.5826-91_5826-90insTC	XP_011536181.1:n.5826-91_5826-90insTC
XR_944868.1:n.485-8485_485-8484insGA
XM_005268629.4:c.7029-91_7029-90insTC	XP_005268686.1:n.7029-91_7029-90insTC
XM_011537877.3:c.7029-91_7029-90insTC	XP_011536179.1:n.7029-91_7029-90insTC
XM_017018787.1:c.3945-91_3945-90insTC	XP_016874276.1:n.3945-91_3945-90insTC
XM_017018788.2:c.3291-91_3291-90insTC	XP_016874277.1:n.3291-91_3291-90insTC
XM_024448833.1:c.5826-91_5826-90insTC	XP_024304601.1:n.5826-91_5826-90insTC
XR_944868.2:n.485-8485_485-8484insGA
NM_198578.4:c.7029-91_7029-90insTC MANE Select	NP_940980.4:n.7029-91_7029-90insTC