Canonical Allele Identifier: CA384415159

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40692265T>C (hg19) ; chr12:g.40298463T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298463T>C , CM000674.2:g.40298463T>C	GRCh38
NC_000012.11:g.40692265T>C , CM000674.1:g.40692265T>C	GRCh37
NC_000012.10:g.38978532T>C	NCBI36
NG_011709.1:g.78453T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3317T>C MANE Select	ENSP00000298910.7:p.Val1106Ala
ENST00000679360.1:c.*2226T>C	ENSP00000505368.1:n.*2226T>C
ENST00000680790.1:c.3062T>C	ENSP00000505335.1:p.Val1021Ala
ENST00000298910.11:c.3317T>C	ENSP00000298910.7:p.Val1106Ala
ENST00000343742.6:c.3317T>C	ENSP00000341930.2:p.Val1106Ala
ENST00000430804.5:c.361T>C
NM_198578.3:c.3317T>C	NP_940980.3:p.Val1106Ala
XM_005268629.2:c.3317T>C	XP_005268686.1:p.Val1106Ala
XM_011537877.1:c.3317T>C	XP_011536179.1:p.Val1106Ala
XM_011537878.1:c.3317T>C	XP_011536180.1:p.Val1106Ala
XM_011537879.1:c.2114T>C	XP_011536181.1:p.Val705Ala
XM_011537880.1:c.3317T>C	XP_011536182.1:p.Val1106Ala
XM_011537881.1:c.3317T>C	XP_011536183.1:p.Val1106Ala
XM_011537882.1:c.3317T>C	XP_011536184.1:p.Val1106Ala
XM_005268629.4:c.3317T>C	XP_005268686.1:p.Val1106Ala
XM_011537877.3:c.3317T>C	XP_011536179.1:p.Val1106Ala
XM_011537881.3:c.3317T>C	XP_011536183.1:p.Val1106Ala
XM_011537882.3:c.3317T>C	XP_011536184.1:p.Val1106Ala
XM_017018786.2:c.3317T>C	XP_016874275.1:p.Val1106Ala
XM_017018787.1:c.233T>C	XP_016874276.1:p.Val78Ala
XM_017018789.2:c.3317T>C	XP_016874278.1:p.Val1106Ala
XM_024448833.1:c.2114T>C	XP_024304601.1:p.Val705Ala
XR_001748574.2:n.3559T>C
NM_198578.4:c.3317T>C MANE Select	NP_940980.4:p.Val1106Ala