Canonical Allele Identifier: CA479247270

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757246G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363444G>C , CM000674.2:g.40363444G>C	GRCh38
NC_000012.11:g.40757246G>C , CM000674.1:g.40757246G>C	GRCh37
NC_000012.10:g.39043513G>C	NCBI36
NG_011709.1:g.143434G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7071G>C MANE Select	ENSP00000298910.7:p.Val2357=
ENST00000636518.1:c.868G>C
ENST00000679360.1:c.*5980G>C	ENSP00000505368.1:n.*5980G>C
ENST00000679532.1:c.2845G>C
ENST00000679683.1:c.861G>C
ENST00000680018.1:c.2516G>C	ENSP00000505347.1:n.2516G>C
ENST00000680422.1:c.4158G>C
ENST00000680425.1:c.2238G>C	ENSP00000506459.1:n.2238G>C
ENST00000680453.1:c.2528G>C
ENST00000680790.1:c.6816G>C	ENSP00000505335.1:p.Val2272=
ENST00000681136.1:n.3055G>C
ENST00000681696.1:c.2754G>C	ENSP00000505871.1:p.Val918=
ENST00000681773.1:n.278G>C
ENST00000298910.11:c.7071G>C	ENSP00000298910.7:p.Val2357=
ENST00000430804.5:c.4367G>C
ENST00000479187.5:n.3752G>C
NM_198578.3:c.7071G>C	NP_940980.3:p.Val2357=
XM_005268629.2:c.7071G>C	XP_005268686.1:p.Val2357=
XM_011537877.1:c.7071G>C	XP_011536179.1:p.Val2357=
XM_011537879.1:c.5868G>C	XP_011536181.1:p.Val1956=
XR_944868.1:n.485-8617C>G
XM_005268629.4:c.7071G>C	XP_005268686.1:p.Val2357=
XM_011537877.3:c.7071G>C	XP_011536179.1:p.Val2357=
XM_017018787.1:c.3987G>C	XP_016874276.1:p.Val1329=
XM_017018788.2:c.3333G>C	XP_016874277.1:p.Val1111=
XM_024448833.1:c.5868G>C	XP_024304601.1:p.Val1956=
XR_944868.2:n.485-8617C>G
NM_198578.4:c.7071G>C MANE Select	NP_940980.4:p.Val2357=