Canonical Allele Identifier: CA2695227901

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220432_1220437del , CM000681.2:g.1220432_1220437del	GRCh38
NC_000019.9:g.1220431_1220436del , CM000681.1:g.1220431_1220436del	GRCh37
NC_000019.8:g.1171431_1171436del	NCBI36
NG_007460.2:g.36026_36031del , LRG_319:g.36026_36031del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.524_529del	ENSP00000490268.2:p.Lys175_Asp176del
ENST00000585748.3:c.152_157del	ENSP00000477641.2:p.Lys51_Asp52del
ENST00000585851.2:c.350_355del	ENSP00000467912.2:p.Lys117_Asp118del
ENST00000326873.12:c.524_529del MANE Select	ENSP00000324856.6:p.Lys175_Asp176del
ENST00000652231.1:c.524_529del	ENSP00000498804.1:p.Lys175_Asp176del
ENST00000326873.11:c.524_529del	ENSP00000324856.6:p.Lys175_Asp176del
ENST00000585851.1:c.350_355del	ENSP00000467912.1:p.Lys117_Asp118del
ENST00000586243.5:c.524_529del	ENSP00000467240.2:p.Lys175_Asp176del
ENST00000586358.5:n.347_352del
ENST00000589152.5:n.614_619del
ENST00000591133.2:n.420_425del
NM_000455.4:c.524_529del , LRG_319t1:c.524_529del	NP_000446.1:p.Lys175_Asp176del
XM_005259617.1:c.524_529del	XP_005259674.1:p.Lys175_Asp176del
XM_005259618.3:c.524_529del	XP_005259675.1:p.Lys175_Asp176del
XM_011528209.1:c.302_307del	XP_011526511.1:p.Lys101_Asp102del
XR_936204.1:n.1149_1154del
XM_005259617.3:c.524_529del	XP_005259674.1:p.Lys175_Asp176del
XM_011528209.2:c.302_307del	XP_011526511.1:p.Lys101_Asp102del
XR_001753738.2:n.1149_1154del
XR_001753739.1:n.1149_1154del
XR_001753740.2:n.1149_1154del
NM_000455.5:c.524_529del MANE Select	NP_000446.1:p.Lys175_Asp176del