Canonical Allele Identifier: CA022663
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 156514
ClinVar RCV Id: RCV000144661
dbSNP Id: rs587783061

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1207062T>G , CM000681.2:g.1207062T>G GRCh38
NC_000019.9:g.1207061T>G , CM000681.1:g.1207061T>G GRCh37
NC_000019.8:g.1158061T>G NCBI36
NG_007460.2:g.22656T>G , LRG_319:g.22656T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.149T>G ENSP00000490268.2:p.Leu50Arg
ENST00000585748.3:c.-82-11355T>G ENSP00000477641.2:n.-82-11355T>G
ENST00000585851.2:c.149T>G ENSP00000467912.2:p.Leu50Arg
ENST00000326873.12:c.149T>G MANE Select ENSP00000324856.6:p.Leu50Arg
ENST00000652231.1:c.149T>G ENSP00000498804.1:p.Leu50Arg
ENST00000326873.11:c.149T>G ENSP00000324856.6:p.Leu50Arg
ENST00000585748.2:c.-82-11355T>G ENSP00000477641.1:n.-82-11355T>G
ENST00000585851.1:c.149T>G ENSP00000467912.1:p.Leu50Arg
ENST00000586243.5:c.149T>G ENSP00000467240.2:p.Leu50Arg
ENST00000589152.5:n.239T>G
ENST00000593219.5:c.149T>G ENSP00000466610.1:p.Leu50Arg
NM_000455.4:c.149T>G , LRG_319t1:c.149T>G NP_000446.1:p.Leu50Arg
XM_005259617.1:c.149T>G XP_005259674.1:p.Leu50Arg
XM_005259618.3:c.149T>G XP_005259675.1:p.Leu50Arg
XM_011528209.1:c.-205T>G XP_011526511.1:n.-205T>G
XR_936204.1:n.774T>G
XM_005259617.3:c.149T>G XP_005259674.1:p.Leu50Arg
XM_011528209.2:c.-205T>G XP_011526511.1:n.-205T>G
XR_001753738.2:n.774T>G
XR_001753739.1:n.774T>G
XR_001753740.2:n.774T>G
NM_000455.5:c.149T>G MANE Select NP_000446.1:p.Leu50Arg