LDH info

Canonical Allele Identifier: CA022848
Gene: STK11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 141198
dbSNP Id: rs140112347

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218495G>A , CM000681.2:g.1218495G>A GRCh38
NC_000019.9:g.1218494G>A , CM000681.1:g.1218494G>A GRCh37
NC_000019.8:g.1169494G>A NCBI36
NG_007460.2:g.34089G>A , LRG_319:g.34089G>A

Transcript Alleles

HGVS Amino-acid change
NM_000455.4:c.369G>A , LRG_319t1:c.369G>A NP_000446.1:p.Gln123=
XM_005259617.1:c.369G>A XP_005259674.1:p.Gln123=
XM_005259618.3:c.369G>A XP_005259675.1:p.Gln123=
XM_011528209.1:c.147G>A XP_011526511.1:p.Gln49=
XR_936204.1:n.994G>A
XM_005259617.3:c.369G>A XP_005259674.1:p.Gln123=
XM_011528209.2:c.147G>A XP_011526511.1:p.Gln49=
XR_001753738.2:n.994G>A
XR_001753739.1:n.994G>A
XR_001753740.2:n.994G>A
NM_000455.5:c.369G>A VV NP_000446.1:p.Gln123=
ENST00000326873.11:c.369G>A ENSP00000324856.6:p.Gln123=
ENST00000585748.2:c.-4G>A ENSP00000477641.1:p.=
ENST00000585851.1:c.291-1878G>A ENSP00000467912.1:p.=
ENST00000586243.5:c.369G>A ENSP00000467240.2:p.Gln123=
ENST00000586358.5:n.192G>A
ENST00000589152.5:n.459G>A
ENST00000593219.5:c.*194G>A ENSP00000466610.1:p.=