Canonical Allele Identifier: CA235349054

Gene: LRRK2

Linked Data

• dbSNP Id: rs552393325
• gnomAD v2: 12-40692581-ATATATATATATATATATATAATATATGTATTATAATATATAATACATATAT-A
• gnomAD v3: 12-40298779-ATATATATATATATATATATAATATATGTATTATAATATATAATACATATAT-A
• gnomAD v4: 12-40298779-ATATATATATATATATATATAATATATGTATTATAATATATAATACATATAT-A
• MyVariant Identifiers: chr12:g.40692582_40692632del (hg19) ; chr12:g.40298780_40298830del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298789_40298839del , CM000674.2:g.40298789_40298839del	GRCh38
NC_000012.11:g.40692591_40692641del , CM000674.1:g.40692591_40692641del	GRCh37
NC_000012.10:g.38978858_38978908del	NCBI36
NG_011709.1:g.78779_78829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3347+296_3348-270del MANE Select	ENSP00000298910.7:n.3347+296_3348-270del
ENST00000679360.1:c.*2256+296_*2257-270del	ENSP00000505368.1:n.*2256+296_*2257-270del
ENST00000680790.1:c.3092+296_3093-270del	ENSP00000505335.1:n.3092+296_3093-270del
ENST00000298910.11:c.3347+296_3348-270del	ENSP00000298910.7:n.3347+296_3348-270del
ENST00000343742.6:c.3347+296_3348-270del	ENSP00000341930.2:n.3347+296_3348-270del
ENST00000430804.5:c.391+296_392-270del
ENST00000479187.5:n.28+296_29-270del
NM_198578.3:c.3347+296_3348-270del	NP_940980.3:n.3347+296_3348-270del
XM_005268629.2:c.3347+296_3348-270del	XP_005268686.1:n.3347+296_3348-270del
XM_011537877.1:c.3347+296_3348-270del	XP_011536179.1:n.3347+296_3348-270del
XM_011537878.1:c.3347+296_3348-270del	XP_011536180.1:n.3347+296_3348-270del
XM_011537879.1:c.2144+296_2145-270del	XP_011536181.1:n.2144+296_2145-270del
XM_011537880.1:c.3347+296_3348-270del	XP_011536182.1:n.3347+296_3348-270del
XM_011537881.1:c.3347+296_3348-270del	XP_011536183.1:n.3347+296_3348-270del
XM_011537882.1:c.3347+296_3348-270del	XP_011536184.1:n.3347+296_3348-270del
XM_005268629.4:c.3347+296_3348-270del	XP_005268686.1:n.3347+296_3348-270del
XM_011537877.3:c.3347+296_3348-270del	XP_011536179.1:n.3347+296_3348-270del
XM_011537881.3:c.3347+296_3348-270del	XP_011536183.1:n.3347+296_3348-270del
XM_011537882.3:c.3347+296_3348-270del	XP_011536184.1:n.3347+296_3348-270del
XM_017018786.2:c.3347+296_3348-270del	XP_016874275.1:n.3347+296_3348-270del
XM_017018787.1:c.263+296_264-270del	XP_016874276.1:n.263+296_264-270del
XM_017018789.2:c.3347+296_3348-270del	XP_016874278.1:n.3347+296_3348-270del
XM_024448833.1:c.2144+296_2145-270del	XP_024304601.1:n.2144+296_2145-270del
XR_001748574.2:n.3589+296_3590-270del
NM_198578.4:c.3347+296_3348-270del MANE Select	NP_940980.4:n.3347+296_3348-270del