Canonical Allele Identifier: CA2317590299
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221215A= , CM000681.2:g.1221215A= GRCh38
NC_000019.9:g.1221214A= , CM000681.1:g.1221214A= GRCh37
NC_000019.8:g.1172214A= NCBI36
NG_007460.2:g.36809A= , LRG_319:g.36809A=

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.737A= ENSP00000490268.2:p.Tyr246=
ENST00000585748.3:c.365A= ENSP00000477641.2:p.Tyr122=
ENST00000585851.2:c.563A= ENSP00000467912.2:p.Tyr188=
ENST00000326873.12:c.737A= MANE Select ENSP00000324856.6:p.Tyr246=
ENST00000652231.1:c.737A= ENSP00000498804.1:p.Tyr246=
ENST00000326873.11:c.737A= ENSP00000324856.6:p.Tyr246=
ENST00000586243.5:c.737A= ENSP00000467240.2:p.Tyr246=
ENST00000586358.5:n.635A=
ENST00000589152.5:n.827A=
ENST00000591133.2:n.708A=
NM_000455.4:c.737A= , LRG_319t1:c.737A= NP_000446.1:p.Tyr246=
XM_005259617.1:c.737A= XP_005259674.1:p.Tyr246=
XM_005259618.3:c.737A= XP_005259675.1:p.Tyr246=
XM_011528209.1:c.515A= XP_011526511.1:p.Tyr172=
XR_936204.1:n.1362A=
XM_005259617.3:c.737A= XP_005259674.1:p.Tyr246=
XM_011528209.2:c.515A= XP_011526511.1:p.Tyr172=
XR_001753738.2:n.1362A=
XR_001753739.1:n.1362A=
XR_001753740.2:n.1362A=
NM_000455.5:c.737A= MANE Select NP_000446.1:p.Tyr246=