Canonical Allele Identifier: CA384414851

Gene: LRRK2

Linked Data

• dbSNP Id: rs1944464021
• gnomAD v3: 12-40298405-C-T
• gnomAD v4: 12-40298405-C-T
• MyVariant Identifiers: chr12:g.40692207C>T (hg19) ; chr12:g.40298405C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298405C>T , CM000674.2:g.40298405C>T	GRCh38
NC_000012.11:g.40692207C>T , CM000674.1:g.40692207C>T	GRCh37
NC_000012.10:g.38978474C>T	NCBI36
NG_011709.1:g.78395C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3259C>T MANE Select	ENSP00000298910.7:p.Gln1087Ter
ENST00000679360.1:c.*2168C>T	ENSP00000505368.1:n.*2168C>T
ENST00000680790.1:c.3004C>T	ENSP00000505335.1:p.Gln1002Ter
ENST00000298910.11:c.3259C>T	ENSP00000298910.7:p.Gln1087Ter
ENST00000343742.6:c.3259C>T	ENSP00000341930.2:p.Gln1087Ter
ENST00000430804.5:c.303C>T
NM_198578.3:c.3259C>T	NP_940980.3:p.Gln1087Ter
XM_005268629.2:c.3259C>T	XP_005268686.1:p.Gln1087Ter
XM_011537877.1:c.3259C>T	XP_011536179.1:p.Gln1087Ter
XM_011537878.1:c.3259C>T	XP_011536180.1:p.Gln1087Ter
XM_011537879.1:c.2056C>T	XP_011536181.1:p.Gln686Ter
XM_011537880.1:c.3259C>T	XP_011536182.1:p.Gln1087Ter
XM_011537881.1:c.3259C>T	XP_011536183.1:p.Gln1087Ter
XM_011537882.1:c.3259C>T	XP_011536184.1:p.Gln1087Ter
XM_005268629.4:c.3259C>T	XP_005268686.1:p.Gln1087Ter
XM_011537877.3:c.3259C>T	XP_011536179.1:p.Gln1087Ter
XM_011537881.3:c.3259C>T	XP_011536183.1:p.Gln1087Ter
XM_011537882.3:c.3259C>T	XP_011536184.1:p.Gln1087Ter
XM_017018786.2:c.3259C>T	XP_016874275.1:p.Gln1087Ter
XM_017018787.1:c.175C>T	XP_016874276.1:p.Gln59Ter
XM_017018789.2:c.3259C>T	XP_016874278.1:p.Gln1087Ter
XM_024448833.1:c.2056C>T	XP_024304601.1:p.Gln686Ter
XR_001748574.2:n.3501C>T
NM_198578.4:c.3259C>T MANE Select	NP_940980.4:p.Gln1087Ter