Canonical Allele Identifier: CA604504569

Gene: LRRK2

Linked Data

• dbSNP Id: rs1161454091
• gnomAD v2: 12-40734579-G-GTT
• gnomAD v3: 12-40340777-G-GTT
• gnomAD v4: 12-40340777-G-GTT
• MyVariant Identifiers: chr12:g.40734579_40734580insTT (hg19) ; chr12:g.40340777_40340778insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340777_40340778insTT , CM000674.2:g.40340777_40340778insTT	GRCh38
NC_000012.11:g.40734579_40734580insTT , CM000674.1:g.40734579_40734580insTT	GRCh37
NC_000012.10:g.39020846_39020847insTT	NCBI36
NG_011709.1:g.120767_120768insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6109+323_6109+324insTT MANE Select	ENSP00000298910.7:n.6109+323_6109+324insTT
ENST00000679360.1:c.*5018+323_*5018+324insTT	ENSP00000505368.1:n.*5018+323_*5018+324insTT
ENST00000679532.1:c.1883+323_1883+324insTT
ENST00000680018.1:c.1554+323_1554+324insTT	ENSP00000505347.1:n.1554+323_1554+324insTT
ENST00000680422.1:c.1754+323_1754+324insTT
ENST00000680425.1:c.1276+323_1276+324insTT	ENSP00000506459.1:n.1276+323_1276+324insTT
ENST00000680453.1:c.1566+323_1566+324insTT
ENST00000680790.1:c.5854+323_5854+324insTT	ENSP00000505335.1:n.5854+323_5854+324insTT
ENST00000681136.1:n.2093+323_2093+324insTT
ENST00000681696.1:c.1792+323_1792+324insTT	ENSP00000505871.1:n.1792+323_1792+324insTT
ENST00000298910.11:c.6109+323_6109+324insTT	ENSP00000298910.7:n.6109+323_6109+324insTT
ENST00000430804.5:c.3405+323_3405+324insTT
ENST00000479187.5:n.2790+323_2790+324insTT
NM_198578.3:c.6109+323_6109+324insTT	NP_940980.3:n.6109+323_6109+324insTT
XM_005268629.2:c.6109+323_6109+324insTT	XP_005268686.1:n.6109+323_6109+324insTT
XM_011537877.1:c.6109+323_6109+324insTT	XP_011536179.1:n.6109+323_6109+324insTT
XM_011537878.1:c.6109+323_6109+324insTT	XP_011536180.1:n.6109+323_6109+324insTT
XM_011537879.1:c.4906+323_4906+324insTT	XP_011536181.1:n.4906+323_4906+324insTT
XM_005268629.4:c.6109+323_6109+324insTT	XP_005268686.1:n.6109+323_6109+324insTT
XM_011537877.3:c.6109+323_6109+324insTT	XP_011536179.1:n.6109+323_6109+324insTT
XM_017018787.1:c.3025+323_3025+324insTT	XP_016874276.1:n.3025+323_3025+324insTT
XM_017018788.2:c.2371+323_2371+324insTT	XP_016874277.1:n.2371+323_2371+324insTT
XM_024448833.1:c.4906+323_4906+324insTT	XP_024304601.1:n.4906+323_4906+324insTT
NM_198578.4:c.6109+323_6109+324insTT MANE Select	NP_940980.4:n.6109+323_6109+324insTT