Canonical Allele Identifier: CA402954111
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs2145436508
gnomAD v4: 19-1226610-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226610G>A , CM000681.2:g.1226610G>A GRCh38
NC_000019.9:g.1226609G>A , CM000681.1:g.1226609G>A GRCh37
NC_000019.8:g.1177609G>A NCBI36
NG_007460.2:g.42204G>A , LRG_319:g.42204G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2866G>A ENSP00000490268.2:n.*2866G>A
ENST00000585748.3:c.893G>A ENSP00000477641.2:p.Ser298Asn
ENST00000585851.2:c.1091G>A ENSP00000467912.2:p.Ser364Asn
ENST00000326873.12:c.1265G>A MANE Select ENSP00000324856.6:p.Ser422Asn
ENST00000326873.11:c.1265G>A ENSP00000324856.6:p.Ser422Asn
ENST00000585465.2:n.2998G>A
ENST00000586243.5:c.1262G>A ENSP00000467240.2:p.Ser421Asn
ENST00000589152.5:n.1963G>A
NM_000455.4:c.1265G>A , LRG_319t1:c.1265G>A NP_000446.1:p.Ser422Asn
XM_005259617.1:c.1260G>A XP_005259674.1:p.Gln420=
XM_011528209.1:c.1038G>A XP_011526511.1:p.Gln346=
XM_005259617.3:c.1260G>A XP_005259674.1:p.Gln420=
XM_011528209.2:c.1038G>A XP_011526511.1:p.Gln346=
XR_001753738.2:n.2071G>A
XR_001753740.2:n.2041G>A
NM_000455.5:c.1265G>A MANE Select NP_000446.1:p.Ser422Asn