Canonical Allele Identifier: CA479247140

Gene: LRRK2

Linked Data

• dbSNP Id: rs1397375920
• gnomAD v2: 12-40757213-T-C
• gnomAD v4: 12-40363411-T-C
• MyVariant Identifiers: chr12:g.40757213T>C (hg19) ; chr12:g.40363411T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363411T>C , CM000674.2:g.40363411T>C	GRCh38
NC_000012.11:g.40757213T>C , CM000674.1:g.40757213T>C	GRCh37
NC_000012.10:g.39043480T>C	NCBI36
NG_011709.1:g.143401T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7038T>C MANE Select	ENSP00000298910.7:p.Tyr2346=
ENST00000636518.1:c.835T>C
ENST00000679360.1:c.*5947T>C	ENSP00000505368.1:n.*5947T>C
ENST00000679532.1:c.2812T>C
ENST00000679683.1:c.828T>C
ENST00000680018.1:c.2483T>C	ENSP00000505347.1:n.2483T>C
ENST00000680422.1:c.4125T>C
ENST00000680425.1:c.2205T>C	ENSP00000506459.1:n.2205T>C
ENST00000680453.1:c.2495T>C
ENST00000680790.1:c.6783T>C	ENSP00000505335.1:p.Tyr2261=
ENST00000681136.1:n.3022T>C
ENST00000681696.1:c.2721T>C	ENSP00000505871.1:p.Tyr907=
ENST00000681773.1:n.245T>C
ENST00000298910.11:c.7038T>C	ENSP00000298910.7:p.Tyr2346=
ENST00000430804.5:c.4334T>C
ENST00000479187.5:n.3719T>C
NM_198578.3:c.7038T>C	NP_940980.3:p.Tyr2346=
XM_005268629.2:c.7038T>C	XP_005268686.1:p.Tyr2346=
XM_011537877.1:c.7038T>C	XP_011536179.1:p.Tyr2346=
XM_011537879.1:c.5835T>C	XP_011536181.1:p.Tyr1945=
XR_944868.1:n.485-8584A>G
XM_005268629.4:c.7038T>C	XP_005268686.1:p.Tyr2346=
XM_011537877.3:c.7038T>C	XP_011536179.1:p.Tyr2346=
XM_017018787.1:c.3954T>C	XP_016874276.1:p.Tyr1318=
XM_017018788.2:c.3300T>C	XP_016874277.1:p.Tyr1100=
XM_024448833.1:c.5835T>C	XP_024304601.1:p.Tyr1945=
XR_944868.2:n.485-8584A>G
NM_198578.4:c.7038T>C MANE Select	NP_940980.4:p.Tyr2346=