Canonical Allele Identifier: CA2317593800
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226629G= , CM000681.2:g.1226629G= GRCh38
NC_000019.9:g.1226628G= , CM000681.1:g.1226628G= GRCh37
NC_000019.8:g.1177628G= NCBI36
NG_007460.2:g.42223G= , LRG_319:g.42223G=

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.*2885G= ENSP00000490268.2:n.*2885G=
ENST00000585748.3:c.912G= ENSP00000477641.2:p.Ser304=
ENST00000585851.2:c.1110G= ENSP00000467912.2:p.Ser370=
ENST00000326873.12:c.1284G= MANE Select ENSP00000324856.6:p.Ser428=
ENST00000326873.11:c.1284G= ENSP00000324856.6:p.Ser428=
ENST00000585465.2:n.3017G=
ENST00000586243.5:c.1281G= ENSP00000467240.2:p.Ser427=
ENST00000589152.5:n.1982G=
NM_000455.4:c.1284G= , LRG_319t1:c.1284G= NP_000446.1:p.Ser428=
XM_005259617.1:c.1279G= XP_005259674.1:p.Gly427=
XM_011528209.1:c.1057G= XP_011526511.1:p.Gly353=
XM_005259617.3:c.1279G= XP_005259674.1:p.Gly427=
XM_011528209.2:c.1057G= XP_011526511.1:p.Gly353=
XR_001753738.2:n.2090G=
XR_001753740.2:n.2060G=
NM_000455.5:c.1284G= MANE Select NP_000446.1:p.Ser428=