Canonical Allele Identifier: CA2695227929

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220628_1220709del , CM000681.2:g.1220628_1220709del	GRCh38
NC_000019.9:g.1220627_1220708del , CM000681.1:g.1220627_1220708del	GRCh37
NC_000019.8:g.1171627_1171708del	NCBI36
NG_007460.2:g.36222_36303del , LRG_319:g.36222_36303del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.645_726del	ENSP00000490268.2:p.Ala218SerfsTer?
ENST00000585748.3:c.273_354del	ENSP00000477641.2:p.Ala94SerfsTer?
ENST00000585851.2:c.471_552del	ENSP00000467912.2:p.Ala160SerfsTer?
ENST00000326873.12:c.645_726del MANE Select	ENSP00000324856.6:p.Ala218SerfsTer?
ENST00000652231.1:c.645_726del	ENSP00000498804.1:p.Ala218SerfsTer?
ENST00000326873.11:c.645_726del	ENSP00000324856.6:p.Ala218SerfsTer?
ENST00000586243.5:c.645_726del	ENSP00000467240.2:p.Ala218SerfsTer?
ENST00000586358.5:n.543_624del
ENST00000589152.5:n.735_816del
ENST00000591133.2:n.616_697del
NM_000455.4:c.645_726del , LRG_319t1:c.645_726del	NP_000446.1:p.Ala218SerfsTer?
XM_005259617.1:c.645_726del	XP_005259674.1:p.Ala218SerfsTer?
XM_005259618.3:c.645_726del	XP_005259675.1:p.Ala218SerfsTer?
XM_011528209.1:c.423_504del	XP_011526511.1:p.Ala144SerfsTer?
XR_936204.1:n.1270_1351del
XM_005259617.3:c.645_726del	XP_005259674.1:p.Ala218SerfsTer?
XM_011528209.2:c.423_504del	XP_011526511.1:p.Ala144SerfsTer?
XR_001753738.2:n.1270_1351del
XR_001753739.1:n.1270_1351del
XR_001753740.2:n.1270_1351del
NM_000455.5:c.645_726del MANE Select	NP_000446.1:p.Ala218SerfsTer?