Canonical Allele Identifier: CA384406491

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40745355G>C (hg19) ; chr12:g.40351553G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351553G>C , CM000674.2:g.40351553G>C	GRCh38
NC_000012.11:g.40745355G>C , CM000674.1:g.40745355G>C	GRCh37
NC_000012.10:g.39031622G>C	NCBI36
NG_011709.1:g.131543G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6396G>C MANE Select	ENSP00000298910.7:p.Leu2132Phe
ENST00000636518.1:c.193G>C
ENST00000679360.1:c.*5305G>C	ENSP00000505368.1:n.*5305G>C
ENST00000679532.1:c.2170G>C
ENST00000679683.1:c.186G>C
ENST00000680018.1:c.1841G>C	ENSP00000505347.1:n.1841G>C
ENST00000680422.1:c.2041G>C
ENST00000680425.1:c.1563G>C	ENSP00000506459.1:n.1563G>C
ENST00000680453.1:c.1853G>C
ENST00000680790.1:c.6141G>C	ENSP00000505335.1:p.Leu2047Phe
ENST00000681136.1:n.2380G>C
ENST00000681696.1:c.2079G>C	ENSP00000505871.1:p.Leu693Phe
ENST00000298910.11:c.6396G>C	ENSP00000298910.7:p.Leu2132Phe
ENST00000430804.5:c.3692G>C
ENST00000479187.5:n.3077G>C
NM_198578.3:c.6396G>C	NP_940980.3:p.Leu2132Phe
XM_005268629.2:c.6396G>C	XP_005268686.1:p.Leu2132Phe
XM_011537877.1:c.6396G>C	XP_011536179.1:p.Leu2132Phe
XM_011537878.1:c.6396G>C	XP_011536180.1:p.Leu2132Phe
XM_011537879.1:c.5193G>C	XP_011536181.1:p.Leu1731Phe
XM_005268629.4:c.6396G>C	XP_005268686.1:p.Leu2132Phe
XM_011537877.3:c.6396G>C	XP_011536179.1:p.Leu2132Phe
XM_017018787.1:c.3312G>C	XP_016874276.1:p.Leu1104Phe
XM_017018788.2:c.2658G>C	XP_016874277.1:p.Leu886Phe
XM_024448833.1:c.5193G>C	XP_024304601.1:p.Leu1731Phe
NM_198578.4:c.6396G>C MANE Select	NP_940980.4:p.Leu2132Phe