Canonical Allele Identifier: CA645602383

Gene: STK11

Linked Data

• COSMIC: COSM166199

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207080_1207081insTTCC , CM000681.2:g.1207080_1207081insTTCC	GRCh38
NC_000019.9:g.1207079_1207080insTTCC , CM000681.1:g.1207079_1207080insTTCC	GRCh37
NC_000019.8:g.1158079_1158080insTTCC	NCBI36
NG_007460.2:g.22674_22675insTTCC , LRG_319:g.22674_22675insTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.167_168insTTCC	ENSP00000490268.2:p.Glu57SerfsTer?
ENST00000585748.3:c.-82-11337_-82-11336insTTCC	ENSP00000477641.2:n.-82-11337_-82-11336insTTCC
ENST00000585851.2:c.167_168insTTCC	ENSP00000467912.2:p.Glu57SerfsTer?
ENST00000326873.12:c.167_168insTTCC MANE Select	ENSP00000324856.6:p.Glu57SerfsTer?
ENST00000652231.1:c.167_168insTTCC	ENSP00000498804.1:p.Glu57SerfsTer?
ENST00000326873.11:c.167_168insTTCC	ENSP00000324856.6:p.Glu57SerfsTer?
ENST00000585748.2:c.-82-11337_-82-11336insTTCC	ENSP00000477641.1:n.-82-11337_-82-11336insTTCC
ENST00000585851.1:c.167_168insTTCC	ENSP00000467912.1:p.Glu57SerfsTer?
ENST00000586243.5:c.167_168insTTCC	ENSP00000467240.2:p.Glu57SerfsTer?
ENST00000589152.5:n.257_258insTTCC
ENST00000593219.5:c.167_168insTTCC	ENSP00000466610.1:p.Glu57SerfsTer?
NM_000455.4:c.167_168insTTCC , LRG_319t1:c.167_168insTTCC	NP_000446.1:p.Glu57SerfsTer?
XM_005259617.1:c.167_168insTTCC	XP_005259674.1:p.Glu57SerfsTer?
XM_005259618.3:c.167_168insTTCC	XP_005259675.1:p.Glu57SerfsTer?
XM_011528209.1:c.-187_-186insTTCC	XP_011526511.1:n.-187_-186insTTCC
XR_936204.1:n.792_793insTTCC
XM_005259617.3:c.167_168insTTCC	XP_005259674.1:p.Glu57SerfsTer?
XM_011528209.2:c.-187_-186insTTCC	XP_011526511.1:n.-187_-186insTTCC
XR_001753738.2:n.792_793insTTCC
XR_001753739.1:n.792_793insTTCC
XR_001753740.2:n.792_793insTTCC
NM_000455.5:c.167_168insTTCC MANE Select	NP_000446.1:p.Glu57SerfsTer?