Canonical Allele Identifier: CA2317589070

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219342_1219343delinsCT , CM000681.2:g.1219342_1219343delinsCT	GRCh38
NC_000019.9:g.1219341_1219342delinsCT , CM000681.1:g.1219341_1219342delinsCT	GRCh37
NC_000019.8:g.1170341_1170342delinsCT	NCBI36
NG_007460.2:g.34936_34937delinsCT , LRG_319:g.34936_34937delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.393_394delinsCT	ENSP00000490268.2:p.Tyr131=
ENST00000585748.3:c.21_22delinsCT	ENSP00000477641.2:p.Tyr7=
ENST00000585851.2:c.291-1031_291-1030delinsCT	ENSP00000467912.2:n.291-1031_291-1030delinsCT
ENST00000326873.12:c.393_394delinsCT MANE Select	ENSP00000324856.6:p.Tyr131=
ENST00000652231.1:c.393_394delinsCT	ENSP00000498804.1:p.Tyr131=
ENST00000326873.11:c.393_394delinsCT	ENSP00000324856.6:p.Tyr131=
ENST00000585748.2:c.21_22delinsCT	ENSP00000477641.1:p.Tyr7=
ENST00000585851.1:c.291-1031_291-1030delinsCT	ENSP00000467912.1:n.291-1031_291-1030delinsCT
ENST00000586243.5:c.393_394delinsCT	ENSP00000467240.2:p.Tyr131=
ENST00000586358.5:n.216_217delinsCT
ENST00000589152.5:n.483_484delinsCT
ENST00000593219.5:c.*218_*219delinsCT	ENSP00000466610.1:n.*218_*219delinsCT
NM_000455.4:c.393_394delinsCT , LRG_319t1:c.393_394delinsCT	NP_000446.1:p.Tyr131=
XM_005259617.1:c.393_394delinsCT	XP_005259674.1:p.Tyr131=
XM_005259618.3:c.393_394delinsCT	XP_005259675.1:p.Tyr131=
XM_011528209.1:c.171_172delinsCT	XP_011526511.1:p.Tyr57=
XR_936204.1:n.1018_1019delinsCT
XM_005259617.3:c.393_394delinsCT	XP_005259674.1:p.Tyr131=
XM_011528209.2:c.171_172delinsCT	XP_011526511.1:p.Tyr57=
XR_001753738.2:n.1018_1019delinsCT
XR_001753739.1:n.1018_1019delinsCT
XR_001753740.2:n.1018_1019delinsCT
NM_000455.5:c.393_394delinsCT MANE Select	NP_000446.1:p.Tyr131=