Canonical Allele Identifier: CA604506182

Gene: LRRK2

Linked Data

• dbSNP Id: rs1170495584
• gnomAD v2: 12-40757138-T-TG
• gnomAD v3: 12-40363336-T-TG
• gnomAD v4: 12-40363336-T-TG
• MyVariant Identifiers: chr12:g.40757138_40757139insG (hg19) ; chr12:g.40363336_40363337insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363336_40363337insG , CM000674.2:g.40363336_40363337insG	GRCh38
NC_000012.11:g.40757138_40757139insG , CM000674.1:g.40757138_40757139insG	GRCh37
NC_000012.10:g.39043405_39043406insG	NCBI36
NG_011709.1:g.143326_143327insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7029-66_7029-65insG MANE Select	ENSP00000298910.7:n.7029-66_7029-65insG
ENST00000636518.1:c.826-66_826-65insG
ENST00000679360.1:c.*5938-66_*5938-65insG	ENSP00000505368.1:n.*5938-66_*5938-65insG...
ENST00000679532.1:c.2803-66_2803-65insG
ENST00000679683.1:c.819-66_819-65insG
ENST00000680018.1:c.2474-66_2474-65insG	ENSP00000505347.1:n.2474-66_2474-65insG
ENST00000680422.1:c.4116-66_4116-65insG
ENST00000680425.1:c.2196-66_2196-65insG	ENSP00000506459.1:n.2196-66_2196-65insG
ENST00000680453.1:c.2486-66_2486-65insG
ENST00000680790.1:c.6774-66_6774-65insG	ENSP00000505335.1:n.6774-66_6774-65insG
ENST00000681136.1:n.3013-66_3013-65insG
ENST00000681696.1:c.2712-66_2712-65insG	ENSP00000505871.1:n.2712-66_2712-65insG
ENST00000681773.1:n.236-66_236-65insG
ENST00000298910.11:c.7029-66_7029-65insG	ENSP00000298910.7:n.7029-66_7029-65insG
ENST00000430804.5:c.4325-66_4325-65insG
ENST00000479187.5:n.3710-66_3710-65insG
NM_198578.3:c.7029-66_7029-65insG	NP_940980.3:n.7029-66_7029-65insG
XM_005268629.2:c.7029-66_7029-65insG	XP_005268686.1:n.7029-66_7029-65insG
XM_011537877.1:c.7029-66_7029-65insG	XP_011536179.1:n.7029-66_7029-65insG
XM_011537879.1:c.5826-66_5826-65insG	XP_011536181.1:n.5826-66_5826-65insG
XR_944868.1:n.485-8510_485-8509insC
XM_005268629.4:c.7029-66_7029-65insG	XP_005268686.1:n.7029-66_7029-65insG
XM_011537877.3:c.7029-66_7029-65insG	XP_011536179.1:n.7029-66_7029-65insG
XM_017018787.1:c.3945-66_3945-65insG	XP_016874276.1:n.3945-66_3945-65insG
XM_017018788.2:c.3291-66_3291-65insG	XP_016874277.1:n.3291-66_3291-65insG
XM_024448833.1:c.5826-66_5826-65insG	XP_024304601.1:n.5826-66_5826-65insG
XR_944868.2:n.485-8510_485-8509insC
NM_198578.4:c.7029-66_7029-65insG MANE Select	NP_940980.4:n.7029-66_7029-65insG