Canonical Allele Identifier: CA2317590773

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221972_1221990delinsAAGAGGTTCTCCATCCGGC , CM000681.2:g.1221972_1221990delinsAAGAGGTTCTCCATCCGGC	GRCh38
NC_000019.9:g.1221971_1221989delinsAAGAGGTTCTCCATCCGGC , CM000681.1:g.1221971_1221989delinsAAGAGGTTCTCCATCCGGC	GRCh37
NC_000019.8:g.1172971_1172989delinsAAGAGGTTCTCCATCCGGC	NCBI36
NG_007460.2:g.37566_37584delinsAAGAGGTTCTCCATCCGGC , LRG_319:g.37566_37584delinsAAGAGGTTCTCCATCCGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.886_904delinsAAGAGGTTCTCCATCCGGC	ENSP00000490268.2:p.Lys296=
ENST00000585748.3:c.514_532delinsAAGAGGTTCTCCATCCGGC	ENSP00000477641.2:p.Lys172=
ENST00000585851.2:c.712_730delinsAAGAGGTTCTCCATCCGGC	ENSP00000467912.2:p.Lys238=
ENST00000326873.12:c.886_904delinsAAGAGGTTCTCCATCCGGC MANE Select	ENSP00000324856.6:p.Lys296=
ENST00000652231.1:c.886_904delinsAAGAGGTTCTCCATCCGGC	ENSP00000498804.1:p.Lys296=
ENST00000326873.11:c.886_904delinsAAGAGGTTCTCCATCCGGC	ENSP00000324856.6:p.Lys296=
ENST00000586243.5:c.886_904delinsAAGAGGTTCTCCATCCGGC	ENSP00000467240.2:p.Lys296=
ENST00000589152.5:n.1584_1602delinsAAGAGGTTCTCCATCCGGC
ENST00000591133.2:n.857_875delinsAAGAGGTTCTCCATCCGGC
NM_000455.4:c.886_904delinsAAGAGGTTCTCCATCCGGC , LRG_319t1:c.886_904delinsAAGAGGTTCTCCATCCGGC	NP_000446.1:p.Lys296=
XM_005259617.1:c.886_904delinsAAGAGGTTCTCCATCCGGC	XP_005259674.1:p.Lys296=
XM_005259618.3:c.886_904delinsAAGAGGTTCTCCATCCGGC	XP_005259675.1:p.Lys296=
XM_011528209.1:c.664_682delinsAAGAGGTTCTCCATCCGGC	XP_011526511.1:p.Lys222=
XR_936204.1:n.1662_1680delinsAAGAGGTTCTCCATCCGGC
XM_005259617.3:c.886_904delinsAAGAGGTTCTCCATCCGGC	XP_005259674.1:p.Lys296=
XM_011528209.2:c.664_682delinsAAGAGGTTCTCCATCCGGC	XP_011526511.1:p.Lys222=
XR_001753738.2:n.1692_1710delinsAAGAGGTTCTCCATCCGGC
XR_001753739.1:n.1692_1710delinsAAGAGGTTCTCCATCCGGC
XR_001753740.2:n.1662_1680delinsAAGAGGTTCTCCATCCGGC
NM_000455.5:c.886_904delinsAAGAGGTTCTCCATCCGGC MANE Select	NP_000446.1:p.Lys296=