Canonical Allele Identifier: CA384406500

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40745357A>C (hg19) ; chr12:g.40351555A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351555A>C , CM000674.2:g.40351555A>C	GRCh38
NC_000012.11:g.40745357A>C , CM000674.1:g.40745357A>C	GRCh37
NC_000012.10:g.39031624A>C	NCBI36
NG_011709.1:g.131545A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6398A>C MANE Select	ENSP00000298910.7:p.Asn2133Thr
ENST00000636518.1:c.195A>C
ENST00000679360.1:c.*5307A>C	ENSP00000505368.1:n.*5307A>C
ENST00000679532.1:c.2172A>C
ENST00000679683.1:c.188A>C
ENST00000680018.1:c.1843A>C	ENSP00000505347.1:n.1843A>C
ENST00000680422.1:c.2043A>C
ENST00000680425.1:c.1565A>C	ENSP00000506459.1:n.1565A>C
ENST00000680453.1:c.1855A>C
ENST00000680790.1:c.6143A>C	ENSP00000505335.1:p.Asn2048Thr
ENST00000681136.1:n.2382A>C
ENST00000681696.1:c.2081A>C	ENSP00000505871.1:p.Asn694Thr
ENST00000298910.11:c.6398A>C	ENSP00000298910.7:p.Asn2133Thr
ENST00000430804.5:c.3694A>C
ENST00000479187.5:n.3079A>C
NM_198578.3:c.6398A>C	NP_940980.3:p.Asn2133Thr
XM_005268629.2:c.6398A>C	XP_005268686.1:p.Asn2133Thr
XM_011537877.1:c.6398A>C	XP_011536179.1:p.Asn2133Thr
XM_011537878.1:c.6398A>C	XP_011536180.1:p.Asn2133Thr
XM_011537879.1:c.5195A>C	XP_011536181.1:p.Asn1732Thr
XM_005268629.4:c.6398A>C	XP_005268686.1:p.Asn2133Thr
XM_011537877.3:c.6398A>C	XP_011536179.1:p.Asn2133Thr
XM_017018787.1:c.3314A>C	XP_016874276.1:p.Asn1105Thr
XM_017018788.2:c.2660A>C	XP_016874277.1:p.Asn887Thr
XM_024448833.1:c.5195A>C	XP_024304601.1:p.Asn1732Thr
NM_198578.4:c.6398A>C MANE Select	NP_940980.4:p.Asn2133Thr