Canonical Allele Identifier: CA645604100

Gene: STK11

Linked Data

• COSMIC: COSM27349

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223103dup , CM000681.2:g.1223103dup	GRCh38
NC_000019.9:g.1223102dup , CM000681.1:g.1223102dup	GRCh37
NC_000019.8:g.1174102dup	NCBI36
NG_007460.2:g.38697dup , LRG_319:g.38697dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1039dup	ENSP00000490268.2:p.Ala347GlyfsTer13
ENST00000585748.3:c.667dup	ENSP00000477641.2:p.Ala223GlyfsTer13
ENST00000585851.2:c.865dup	ENSP00000467912.2:p.Ala289GlyfsTer13
ENST00000326873.12:c.1039dup MANE Select	ENSP00000324856.6:p.Ala347GlyfsTer13
ENST00000652231.1:c.1039dup	ENSP00000498804.1:p.Ala347GlyfsTer13
ENST00000326873.11:c.1039dup	ENSP00000324856.6:p.Ala347GlyfsTer13
ENST00000586243.5:c.1039dup	ENSP00000467240.2:p.Ala347GlyfsTer13
ENST00000589152.5:n.1737dup
ENST00000591133.2:n.1010dup
NM_000455.4:c.1039dup , LRG_319t1:c.1039dup	NP_000446.1:p.Ala347GlyfsTer13
XM_005259617.1:c.1039dup	XP_005259674.1:p.Ala347GlyfsTer13
XM_005259618.3:c.1039dup	XP_005259675.1:p.Ala347GlyfsTer13
XM_011528209.1:c.817dup	XP_011526511.1:p.Ala273GlyfsTer13
XR_936204.1:n.1815dup
XM_005259617.3:c.1039dup	XP_005259674.1:p.Ala347GlyfsTer13
XM_011528209.2:c.817dup	XP_011526511.1:p.Ala273GlyfsTer13
XR_001753738.2:n.1845dup
XR_001753739.1:n.1845dup
XR_001753740.2:n.1815dup
NM_000455.5:c.1039dup MANE Select	NP_000446.1:p.Ala347GlyfsTer13