Canonical Allele Identifier: CA2317593804
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226635C= , CM000681.2:g.1226635C= GRCh38
NC_000019.9:g.1226634C= , CM000681.1:g.1226634C= GRCh37
NC_000019.8:g.1177634C= NCBI36
NG_007460.2:g.42229C= , LRG_319:g.42229C=

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.*2891C= ENSP00000490268.2:n.*2891C=
ENST00000585748.3:c.918C= ENSP00000477641.2:p.Cys306=
ENST00000585851.2:c.1116C= ENSP00000467912.2:p.Cys372=
ENST00000326873.12:c.1290C= MANE Select ENSP00000324856.6:p.Cys430=
ENST00000326873.11:c.1290C= ENSP00000324856.6:p.Cys430=
ENST00000585465.2:n.3023C=
ENST00000586243.5:c.1287C= ENSP00000467240.2:p.Cys429=
ENST00000589152.5:n.1988C=
NM_000455.4:c.1290C= , LRG_319t1:c.1290C= NP_000446.1:p.Cys430=
XM_005259617.1:c.1285C= XP_005259674.1:p.Gln429=
XM_011528209.1:c.1063C= XP_011526511.1:p.Gln355=
XM_005259617.3:c.1285C= XP_005259674.1:p.Gln429=
XM_011528209.2:c.1063C= XP_011526511.1:p.Gln355=
XR_001753738.2:n.2096C=
XR_001753740.2:n.2066C=
NM_000455.5:c.1290C= MANE Select NP_000446.1:p.Cys430=