Canonical Allele Identifier: CA479236905
Gene: LRRK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.40657619A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40263817A>T , CM000674.2:g.40263817A>T GRCh38
NC_000012.11:g.40657619A>T , CM000674.1:g.40657619A>T GRCh37
NC_000012.10:g.38943886A>T NCBI36
NG_011709.1:g.43807A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.1572A>T MANE Select ENSP00000298910.7:p.Thr524=
ENST00000679360.1:c.*481A>T ENSP00000505368.1:n.*481A>T
ENST00000680790.1:c.1317A>T ENSP00000505335.1:p.Thr439=
ENST00000298910.11:c.1572A>T ENSP00000298910.7:p.Thr524=
ENST00000343742.6:c.1572A>T ENSP00000341930.2:p.Thr524=
ENST00000416796.5:c.816A>T ENSP00000398726.1:p.Thr272=
NM_198578.3:c.1572A>T NP_940980.3:p.Thr524=
XM_005268629.2:c.1572A>T XP_005268686.1:p.Thr524=
XM_011537877.1:c.1572A>T XP_011536179.1:p.Thr524=
XM_011537878.1:c.1572A>T XP_011536180.1:p.Thr524=
XM_011537879.1:c.369A>T XP_011536181.1:p.Thr123=
XM_011537880.1:c.1572A>T XP_011536182.1:p.Thr524=
XM_011537881.1:c.1572A>T XP_011536183.1:p.Thr524=
XM_011537882.1:c.1572A>T XP_011536184.1:p.Thr524=
XM_005268629.4:c.1572A>T XP_005268686.1:p.Thr524=
XM_011537877.3:c.1572A>T XP_011536179.1:p.Thr524=
XM_011537881.3:c.1572A>T XP_011536183.1:p.Thr524=
XM_011537882.3:c.1572A>T XP_011536184.1:p.Thr524=
XM_017018786.2:c.1572A>T XP_016874275.1:p.Thr524=
XM_017018789.2:c.1572A>T XP_016874278.1:p.Thr524=
XM_024448833.1:c.369A>T XP_024304601.1:p.Thr123=
XR_001748574.2:n.1814A>T
NM_198578.4:c.1572A>T MANE Select NP_940980.4:p.Thr524=