Canonical Allele Identifier: CA2695227949

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221222del , CM000681.2:g.1221222del	GRCh38
NC_000019.9:g.1221221del , CM000681.1:g.1221221del	GRCh37
NC_000019.8:g.1172221del	NCBI36
NG_007460.2:g.36816del , LRG_319:g.36816del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.744del	ENSP00000490268.2:p.Thr249ProfsTer?
ENST00000585748.3:c.372del	ENSP00000477641.2:p.Thr125ProfsTer?
ENST00000585851.2:c.570del	ENSP00000467912.2:p.Thr191ProfsTer?
ENST00000326873.12:c.744del MANE Select	ENSP00000324856.6:p.Thr249ProfsTer?
ENST00000652231.1:c.744del	ENSP00000498804.1:p.Thr249ProfsTer?
ENST00000326873.11:c.744del	ENSP00000324856.6:p.Thr249ProfsTer?
ENST00000586243.5:c.744del	ENSP00000467240.2:p.Thr249ProfsTer?
ENST00000586358.5:n.642del
ENST00000589152.5:n.834del
ENST00000591133.2:n.715del
NM_000455.4:c.744del , LRG_319t1:c.744del	NP_000446.1:p.Thr249ProfsTer?
XM_005259617.1:c.744del	XP_005259674.1:p.Thr249ProfsTer?
XM_005259618.3:c.744del	XP_005259675.1:p.Thr249ProfsTer?
XM_011528209.1:c.522del	XP_011526511.1:p.Thr175ProfsTer?
XR_936204.1:n.1369del
XM_005259617.3:c.744del	XP_005259674.1:p.Thr249ProfsTer?
XM_011528209.2:c.522del	XP_011526511.1:p.Thr175ProfsTer?
XR_001753738.2:n.1369del
XR_001753739.1:n.1369del
XR_001753740.2:n.1369del
NM_000455.5:c.744del MANE Select	NP_000446.1:p.Thr249ProfsTer?