Canonical Allele Identifier: CA402949483
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 490167
dbSNP Id: rs1555738372
gnomAD v4: 19-1220605-G-A
COSMIC: COSM21356

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220605G>A , CM000681.2:g.1220605G>A GRCh38
NC_000019.9:g.1220604G>A , CM000681.1:g.1220604G>A GRCh37
NC_000019.8:g.1171604G>A NCBI36
NG_007460.2:g.36199G>A , LRG_319:g.36199G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.622G>A ENSP00000490268.2:p.Asp208Asn
ENST00000585748.3:c.250G>A ENSP00000477641.2:p.Asp84Asn
ENST00000585851.2:c.448G>A ENSP00000467912.2:p.Asp150Asn
ENST00000326873.12:c.622G>A MANE Select ENSP00000324856.6:p.Asp208Asn
ENST00000652231.1:c.622G>A ENSP00000498804.1:p.Asp208Asn
ENST00000326873.11:c.622G>A ENSP00000324856.6:p.Asp208Asn
ENST00000585851.1:c.448G>A ENSP00000467912.1:p.Asp150Asn
ENST00000586243.5:c.622G>A ENSP00000467240.2:p.Asp208Asn
ENST00000586358.5:n.520G>A
ENST00000589152.5:n.712G>A
ENST00000591133.2:n.593G>A
NM_000455.4:c.622G>A , LRG_319t1:c.622G>A NP_000446.1:p.Asp208Asn
XM_005259617.1:c.622G>A XP_005259674.1:p.Asp208Asn
XM_005259618.3:c.622G>A XP_005259675.1:p.Asp208Asn
XM_011528209.1:c.400G>A XP_011526511.1:p.Asp134Asn
XR_936204.1:n.1247G>A
XM_005259617.3:c.622G>A XP_005259674.1:p.Asp208Asn
XM_011528209.2:c.400G>A XP_011526511.1:p.Asp134Asn
XR_001753738.2:n.1247G>A
XR_001753739.1:n.1247G>A
XR_001753740.2:n.1247G>A
NM_000455.5:c.622G>A MANE Select NP_000446.1:p.Asp208Asn