LDH info

Canonical Allele Identifier: CA384403984
Gene: LRRK2 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340401G>C , CM000674.2:g.40340401G>C GRCh38
NC_000012.11:g.40734203G>C , CM000674.1:g.40734203G>C GRCh37
NC_000012.10:g.39020470G>C NCBI36
NG_011709.1:g.120391G>C

Transcript Alleles

HGVS Amino-acid change
NM_198578.3:c.6056G>C VV NP_940980.3:p.Gly2019Ala
XM_005268629.2:c.6056G>C XP_005268686.1:p.Gly2019Ala
XM_011537877.1:c.6056G>C XP_011536179.1:p.Gly2019Ala
XM_011537878.1:c.6056G>C XP_011536180.1:p.Gly2019Ala
XM_011537879.1:c.4853G>C XP_011536181.1:p.Gly1618Ala
XM_005268629.4:c.6056G>C XP_005268686.1:p.Gly2019Ala
XM_011537877.3:c.6056G>C XP_011536179.1:p.Gly2019Ala
XM_017018787.1:c.2972G>C XP_016874276.1:p.Gly991Ala
XM_017018788.2:c.2318G>C XP_016874277.1:p.Gly773Ala
XM_024448833.1:c.4853G>C XP_024304601.1:p.Gly1618Ala
NM_198578.4:c.6056G>C VV MANE Preferred NP_940980.4:p.Gly2019Ala
ENST00000298910.11:c.6056G>C ENSP00000298910.7:p.Gly2019Ala
ENST00000430804.5:n.3352G>C
ENST00000479187.5:n.2737G>C