Canonical Allele Identifier: CA2695227848

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207034_1207052delinsTT , CM000681.2:g.1207034_1207052delinsTT	GRCh38
NC_000019.9:g.1207033_1207051delinsTT , CM000681.1:g.1207033_1207051delinsTT	GRCh37
NC_000019.8:g.1158033_1158051delinsTT	NCBI36
NG_007460.2:g.22628_22646delinsTT , LRG_319:g.22628_22646delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.121_139delinsTT	ENSP00000490268.2:p.Lys41LeufsTer?
ENST00000585748.3:c.-82-11383_-82-11365delinsTT	ENSP00000477641.2:n.-82-11383_-82-11365de...
ENST00000585851.2:c.121_139delinsTT	ENSP00000467912.2:p.Lys41LeufsTer?
ENST00000326873.12:c.121_139delinsTT MANE Select	ENSP00000324856.6:p.Lys41LeufsTer?
ENST00000652231.1:c.121_139delinsTT	ENSP00000498804.1:p.Lys41LeufsTer?
ENST00000326873.11:c.121_139delinsTT	ENSP00000324856.6:p.Lys41LeufsTer?
ENST00000585748.2:c.-82-11383_-82-11365delinsTT	ENSP00000477641.1:n.-82-11383_-82-11365de...
ENST00000585851.1:c.121_139delinsTT	ENSP00000467912.1:p.Lys41LeufsTer?
ENST00000586243.5:c.121_139delinsTT	ENSP00000467240.2:p.Lys41LeufsTer?
ENST00000589152.5:n.211_229delinsTT
ENST00000593219.5:c.121_139delinsTT	ENSP00000466610.1:p.Lys41LeufsTer?
NM_000455.4:c.121_139delinsTT , LRG_319t1:c.121_139delinsTT	NP_000446.1:p.Lys41LeufsTer?
XM_005259617.1:c.121_139delinsTT	XP_005259674.1:p.Lys41LeufsTer?
XM_005259618.3:c.121_139delinsTT	XP_005259675.1:p.Lys41LeufsTer?
XM_011528209.1:c.-233_-215delinsTT	XP_011526511.1:n.-233_-215delinsTT
XR_936204.1:n.746_764delinsTT
XM_005259617.3:c.121_139delinsTT	XP_005259674.1:p.Lys41LeufsTer?
XM_011528209.2:c.-233_-215delinsTT	XP_011526511.1:n.-233_-215delinsTT
XR_001753738.2:n.746_764delinsTT
XR_001753739.1:n.746_764delinsTT
XR_001753740.2:n.746_764delinsTT
NM_000455.5:c.121_139delinsTT MANE Select	NP_000446.1:p.Lys41LeufsTer?