Canonical Allele Identifier: CA688734067

Gene: LRRK2

Linked Data

• dbSNP Id: rs1555196693
• gnomAD v3: 12-40363312-A-ACACG
• gnomAD v4: 12-40363312-A-ACACG
• MyVariant Identifiers: chr12:g.40757114_40757115insCACG (hg19) ; chr12:g.40363312_40363313insCACG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363314_40363315insCGCA , CM000674.2:g.40363314_40363315insCGCA	GRCh38
NC_000012.11:g.40757116_40757117insCGCA , CM000674.1:g.40757116_40757117insCGCA	GRCh37
NC_000012.10:g.39043383_39043384insCGCA	NCBI36
NG_011709.1:g.143304_143305insCGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7029-88_7029-87insCGCA MANE Select	ENSP00000298910.7:n.7029-88_7029-87insCGCA
ENST00000636518.1:c.826-88_826-87insCGCA
ENST00000679360.1:c.*5938-88_*5938-87insCGCA	ENSP00000505368.1:n.*5938-88_*5938-87insCGCA
ENST00000679532.1:c.2803-88_2803-87insCGCA
ENST00000679683.1:c.819-88_819-87insCGCA
ENST00000680018.1:c.2474-88_2474-87insCGCA	ENSP00000505347.1:n.2474-88_2474-87insCGCA
ENST00000680422.1:c.4116-88_4116-87insCGCA
ENST00000680425.1:c.2196-88_2196-87insCGCA	ENSP00000506459.1:n.2196-88_2196-87insCGCA
ENST00000680453.1:c.2486-88_2486-87insCGCA
ENST00000680790.1:c.6774-88_6774-87insCGCA	ENSP00000505335.1:n.6774-88_6774-87insCGCA
ENST00000681136.1:n.3013-88_3013-87insCGCA
ENST00000681696.1:c.2712-88_2712-87insCGCA	ENSP00000505871.1:n.2712-88_2712-87insCGCA
ENST00000681773.1:n.236-88_236-87insCGCA
ENST00000298910.11:c.7029-88_7029-87insCGCA	ENSP00000298910.7:n.7029-88_7029-87insCGCA
ENST00000430804.5:c.4325-88_4325-87insCGCA
ENST00000479187.5:n.3710-88_3710-87insCGCA
NM_198578.3:c.7029-88_7029-87insCGCA	NP_940980.3:n.7029-88_7029-87insCGCA
XM_005268629.2:c.7029-88_7029-87insCGCA	XP_005268686.1:n.7029-88_7029-87insCGCA
XM_011537877.1:c.7029-88_7029-87insCGCA	XP_011536179.1:n.7029-88_7029-87insCGCA
XM_011537878.1:c.*789_*790insCGCA	XP_011536180.1:n.*789_*790insCGCA
XM_011537879.1:c.5826-88_5826-87insCGCA	XP_011536181.1:n.5826-88_5826-87insCGCA
XR_944868.1:n.485-8486_485-8485insCGTG
XM_005268629.4:c.7029-88_7029-87insCGCA	XP_005268686.1:n.7029-88_7029-87insCGCA
XM_011537877.3:c.7029-88_7029-87insCGCA	XP_011536179.1:n.7029-88_7029-87insCGCA
XM_017018787.1:c.3945-88_3945-87insCGCA	XP_016874276.1:n.3945-88_3945-87insCGCA
XM_017018788.2:c.3291-88_3291-87insCGCA	XP_016874277.1:n.3291-88_3291-87insCGCA
XM_024448833.1:c.5826-88_5826-87insCGCA	XP_024304601.1:n.5826-88_5826-87insCGCA
XR_944868.2:n.485-8486_485-8485insCGTG
NM_198578.4:c.7029-88_7029-87insCGCA MANE Select	NP_940980.4:n.7029-88_7029-87insCGCA