Canonical Allele Identifier: CA688717226

Gene: LRRK2

Linked Data

• dbSNP Id: rs1485268496
• gnomAD v3: 12-40298796-T-TATATATAA
• gnomAD v4: 12-40298796-T-TATATATAA
• MyVariant Identifiers: chr12:g.40692598_40692599insATATATAA (hg19) ; chr12:g.40298796_40298797insATATATAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298799_40298800insTATAAATA , CM000674.2:g.40298799_40298800insTATAAATA	GRCh38
NC_000012.11:g.40692601_40692602insTATAAATA , CM000674.1:g.40692601_40692602insTATAAATA	GRCh37
NC_000012.10:g.38978868_38978869insTATAAATA	NCBI36
NG_011709.1:g.78789_78790insTATAAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3347+306_3347+307insTATAAATA MANE Select	ENSP00000298910.7:n.3347+306_3347+307insTATAAATA
ENST00000679360.1:c.*2256+306_*2256+307insTATAAATA	ENSP00000505368.1:n.*2256+306_*2256+307insTATAAATA
ENST00000680790.1:c.3092+306_3092+307insTATAAATA	ENSP00000505335.1:n.3092+306_3092+307insTATAAATA
ENST00000298910.11:c.3347+306_3347+307insTATAAATA	ENSP00000298910.7:n.3347+306_3347+307insTATAAATA
ENST00000343742.6:c.3347+306_3347+307insTATAAATA	ENSP00000341930.2:n.3347+306_3347+307insTATAAATA
ENST00000430804.5:c.391+306_391+307insTATAAATA
ENST00000479187.5:n.28+306_28+307insTATAAATA
NM_198578.3:c.3347+306_3347+307insTATAAATA	NP_940980.3:n.3347+306_3347+307insTATAAATA
XM_005268629.2:c.3347+306_3347+307insTATAAATA	XP_005268686.1:n.3347+306_3347+307insTATAAATA
XM_011537877.1:c.3347+306_3347+307insTATAAATA	XP_011536179.1:n.3347+306_3347+307insTATAAATA
XM_011537878.1:c.3347+306_3347+307insTATAAATA	XP_011536180.1:n.3347+306_3347+307insTATAAATA
XM_011537879.1:c.2144+306_2144+307insTATAAATA	XP_011536181.1:n.2144+306_2144+307insTATAAATA
XM_011537880.1:c.3347+306_3347+307insTATAAATA	XP_011536182.1:n.3347+306_3347+307insTATAAATA
XM_011537881.1:c.3347+306_3347+307insTATAAATA	XP_011536183.1:n.3347+306_3347+307insTATAAATA
XM_011537882.1:c.3347+306_3347+307insTATAAATA	XP_011536184.1:n.3347+306_3347+307insTATAAATA
XM_005268629.4:c.3347+306_3347+307insTATAAATA	XP_005268686.1:n.3347+306_3347+307insTATAAATA
XM_011537877.3:c.3347+306_3347+307insTATAAATA	XP_011536179.1:n.3347+306_3347+307insTATAAATA
XM_011537881.3:c.3347+306_3347+307insTATAAATA	XP_011536183.1:n.3347+306_3347+307insTATAAATA
XM_011537882.3:c.3347+306_3347+307insTATAAATA	XP_011536184.1:n.3347+306_3347+307insTATAAATA
XM_017018786.2:c.3347+306_3347+307insTATAAATA	XP_016874275.1:n.3347+306_3347+307insTATAAATA
XM_017018787.1:c.263+306_263+307insTATAAATA	XP_016874276.1:n.263+306_263+307insTATAAATA
XM_017018789.2:c.3347+306_3347+307insTATAAATA	XP_016874278.1:n.3347+306_3347+307insTATAAATA
XM_024448833.1:c.2144+306_2144+307insTATAAATA	XP_024304601.1:n.2144+306_2144+307insTATAAATA
XR_001748574.2:n.3589+306_3589+307insTATAAATA
NM_198578.4:c.3347+306_3347+307insTATAAATA MANE Select	NP_940980.4:n.3347+306_3347+307insTATAAATA