Canonical Allele Identifier: CA235349297

Gene: LRRK2

Linked Data

• dbSNP Id: rs1004806263
• gnomAD v2: 12-40692852-T-C
• gnomAD v3: 12-40299050-T-C
• gnomAD v4: 12-40299050-T-C
• MyVariant Identifiers: chr12:g.40692852T>C (hg19) ; chr12:g.40299050T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40299050T>C , CM000674.2:g.40299050T>C	GRCh38
NC_000012.11:g.40692852T>C , CM000674.1:g.40692852T>C	GRCh37
NC_000012.10:g.38979119T>C	NCBI36
NG_011709.1:g.79040T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.3348-59T>C MANE Select	ENSP00000298910.7:n.3348-59T>C
ENST00000679360.1:c.*2257-59T>C	ENSP00000505368.1:n.*2257-59T>C
ENST00000680790.1:c.3093-59T>C	ENSP00000505335.1:n.3093-59T>C
ENST00000298910.11:c.3348-59T>C	ENSP00000298910.7:n.3348-59T>C
ENST00000343742.6:c.3348-59T>C	ENSP00000341930.2:n.3348-59T>C
ENST00000430804.5:c.392-59T>C
ENST00000479187.5:n.29-59T>C
NM_198578.3:c.3348-59T>C	NP_940980.3:n.3348-59T>C
XM_005268629.2:c.3348-59T>C	XP_005268686.1:n.3348-59T>C
XM_011537877.1:c.3348-59T>C	XP_011536179.1:n.3348-59T>C
XM_011537878.1:c.3348-59T>C	XP_011536180.1:n.3348-59T>C
XM_011537879.1:c.2145-59T>C	XP_011536181.1:n.2145-59T>C
XM_011537880.1:c.3348-59T>C	XP_011536182.1:n.3348-59T>C
XM_011537881.1:c.3348-59T>C	XP_011536183.1:n.3348-59T>C
XM_011537882.1:c.3348-59T>C	XP_011536184.1:n.3348-59T>C
XM_005268629.4:c.3348-59T>C	XP_005268686.1:n.3348-59T>C
XM_011537877.3:c.3348-59T>C	XP_011536179.1:n.3348-59T>C
XM_011537881.3:c.3348-59T>C	XP_011536183.1:n.3348-59T>C
XM_011537882.3:c.3348-59T>C	XP_011536184.1:n.3348-59T>C
XM_017018786.2:c.3348-59T>C	XP_016874275.1:n.3348-59T>C
XM_017018787.1:c.264-59T>C	XP_016874276.1:n.264-59T>C
XM_017018789.2:c.3348-59T>C	XP_016874278.1:n.3348-59T>C
XM_024448833.1:c.2145-59T>C	XP_024304601.1:n.2145-59T>C
XR_001748574.2:n.3590-59T>C
NM_198578.4:c.3348-59T>C MANE Select	NP_940980.4:n.3348-59T>C