Canonical Allele Identifier: CA384403816

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734169A>C (hg19) ; chr12:g.40340367A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340367A>C , CM000674.2:g.40340367A>C	GRCh38
NC_000012.11:g.40734169A>C , CM000674.1:g.40734169A>C	GRCh37
NC_000012.10:g.39020436A>C	NCBI36
NG_011709.1:g.120357A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6022A>C MANE Select	ENSP00000298910.7:p.Asn2008His
ENST00000679360.1:c.*4931A>C	ENSP00000505368.1:n.*4931A>C
ENST00000679532.1:c.1796A>C
ENST00000680018.1:c.1467A>C	ENSP00000505347.1:n.1467A>C
ENST00000680422.1:c.1667A>C
ENST00000680425.1:c.1189A>C	ENSP00000506459.1:n.1189A>C
ENST00000680453.1:c.1479A>C
ENST00000680790.1:c.5767A>C	ENSP00000505335.1:p.Asn1923His
ENST00000681136.1:n.2006A>C
ENST00000681696.1:c.1705A>C	ENSP00000505871.1:p.Asn569His
ENST00000298910.11:c.6022A>C	ENSP00000298910.7:p.Asn2008His
ENST00000430804.5:c.3318A>C
ENST00000479187.5:n.2703A>C
NM_198578.3:c.6022A>C	NP_940980.3:p.Asn2008His
XM_005268629.2:c.6022A>C	XP_005268686.1:p.Asn2008His
XM_011537877.1:c.6022A>C	XP_011536179.1:p.Asn2008His
XM_011537878.1:c.6022A>C	XP_011536180.1:p.Asn2008His
XM_011537879.1:c.4819A>C	XP_011536181.1:p.Asn1607His
XM_005268629.4:c.6022A>C	XP_005268686.1:p.Asn2008His
XM_011537877.3:c.6022A>C	XP_011536179.1:p.Asn2008His
XM_017018787.1:c.2938A>C	XP_016874276.1:p.Asn980His
XM_017018788.2:c.2284A>C	XP_016874277.1:p.Asn762His
XM_024448833.1:c.4819A>C	XP_024304601.1:p.Asn1607His
NM_198578.4:c.6022A>C MANE Select	NP_940980.4:p.Asn2008His