LDH info

Canonical Allele Identifier: CA16043164
Gene: STK11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372522
dbSNP Id: rs1057517830

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221212G>A , CM000681.2:g.1221212G>A GRCh38
NC_000019.9:g.1221211G>A , CM000681.1:g.1221211G>A GRCh37
NC_000019.8:g.1172211G>A NCBI36
NG_007460.2:g.36806G>A , LRG_319:g.36806G>A

Transcript Alleles

HGVS Amino-acid change
NM_000455.4:c.735-1G>A , LRG_319t1:c.735-1G>A NP_000446.1:p.=
XM_005259617.1:c.735-1G>A XP_005259674.1:p.=
XM_005259618.3:c.735-1G>A XP_005259675.1:p.=
XM_011528209.1:c.513-1G>A XP_011526511.1:p.=
XR_936204.1:n.1360-1G>A
XM_005259617.3:c.735-1G>A XP_005259674.1:p.=
XM_011528209.2:c.513-1G>A XP_011526511.1:p.=
XR_001753738.2:n.1360-1G>A
XR_001753739.1:n.1360-1G>A
XR_001753740.2:n.1360-1G>A
NM_000455.5:c.735-1G>A VV MANE Preferred NP_000446.1:p.=
ENST00000326873.11:c.735-1G>A ENSP00000324856.6:p.=
ENST00000586243.5:c.735-1G>A ENSP00000467240.2:p.=
ENST00000586358.5:n.633-1G>A
ENST00000589152.5:n.825-1G>A
ENST00000591133.2:n.706-1G>A