Canonical Allele Identifier: CA235349224

Gene: LRRK2

Linked Data

• dbSNP Id: rs10655197
• MyVariant Identifiers: chr12:g.40692688_40692689insCTA (hg19) ; chr12:g.40298886_40298887insCTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298886_40298887insCTA , CM000674.2:g.40298886_40298887insCTA	GRCh38
NC_000012.11:g.40692688_40692689insCTA , CM000674.1:g.40692688_40692689insCTA	GRCh37
NC_000012.10:g.38978955_38978956insCTA	NCBI36
NG_011709.1:g.78876_78877insCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3348-223_3348-222insCTA MANE Select	ENSP00000298910.7:n.3348-223_3348-222insCTA
ENST00000679360.1:c.*2257-223_*2257-222insCTA	ENSP00000505368.1:n.*2257-223_*2257-222insCTA
ENST00000680790.1:c.3093-223_3093-222insCTA	ENSP00000505335.1:n.3093-223_3093-222insCTA
ENST00000298910.11:c.3348-223_3348-222insCTA	ENSP00000298910.7:n.3348-223_3348-222insCTA
ENST00000343742.6:c.3348-223_3348-222insCTA	ENSP00000341930.2:n.3348-223_3348-222insCTA
ENST00000430804.5:c.392-223_392-222insCTA
ENST00000479187.5:n.29-223_29-222insCTA
NM_198578.3:c.3348-223_3348-222insCTA	NP_940980.3:n.3348-223_3348-222insCTA
XM_005268629.2:c.3348-223_3348-222insCTA	XP_005268686.1:n.3348-223_3348-222insCTA
XM_011537877.1:c.3348-223_3348-222insCTA	XP_011536179.1:n.3348-223_3348-222insCTA
XM_011537878.1:c.3348-223_3348-222insCTA	XP_011536180.1:n.3348-223_3348-222insCTA
XM_011537879.1:c.2145-223_2145-222insCTA	XP_011536181.1:n.2145-223_2145-222insCTA
XM_011537880.1:c.3348-223_3348-222insCTA	XP_011536182.1:n.3348-223_3348-222insCTA
XM_011537881.1:c.3348-223_3348-222insCTA	XP_011536183.1:n.3348-223_3348-222insCTA
XM_011537882.1:c.3348-223_3348-222insCTA	XP_011536184.1:n.3348-223_3348-222insCTA
XM_005268629.4:c.3348-223_3348-222insCTA	XP_005268686.1:n.3348-223_3348-222insCTA
XM_011537877.3:c.3348-223_3348-222insCTA	XP_011536179.1:n.3348-223_3348-222insCTA
XM_011537881.3:c.3348-223_3348-222insCTA	XP_011536183.1:n.3348-223_3348-222insCTA
XM_011537882.3:c.3348-223_3348-222insCTA	XP_011536184.1:n.3348-223_3348-222insCTA
XM_017018786.2:c.3348-223_3348-222insCTA	XP_016874275.1:n.3348-223_3348-222insCTA
XM_017018787.1:c.264-223_264-222insCTA	XP_016874276.1:n.264-223_264-222insCTA
XM_017018789.2:c.3348-223_3348-222insCTA	XP_016874278.1:n.3348-223_3348-222insCTA
XM_024448833.1:c.2145-223_2145-222insCTA	XP_024304601.1:n.2145-223_2145-222insCTA
XR_001748574.2:n.3590-223_3590-222insCTA
NM_198578.4:c.3348-223_3348-222insCTA MANE Select	NP_940980.4:n.3348-223_3348-222insCTA