Canonical Allele Identifier: CA2317588689

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218699_1218700delinsGC , CM000681.2:g.1218699_1218700delinsGC	GRCh38
NC_000019.9:g.1218698_1218699delinsGC , CM000681.1:g.1218698_1218699delinsGC	GRCh37
NC_000019.8:g.1169698_1169699delinsGC	NCBI36
NG_007460.2:g.34293_34294delinsGC , LRG_319:g.34293_34294delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+199_374+200delinsGC	ENSP00000490268.2:n.374+199_374+200delinsGC
ENST00000585748.3:c.2+199_2+200delinsGC	ENSP00000477641.2:n.2+199_2+200delinsGC
ENST00000585851.2:c.291-1674_291-1673delinsGC	ENSP00000467912.2:n.291-1674_291-1673delinsGC
ENST00000326873.12:c.374+199_374+200delinsGC MANE Select	ENSP00000324856.6:n.374+199_374+200delinsGC
ENST00000652231.1:c.374+199_374+200delinsGC	ENSP00000498804.1:n.374+199_374+200delinsGC
ENST00000326873.11:c.374+199_374+200delinsGC	ENSP00000324856.6:n.374+199_374+200delinsGC
ENST00000585748.2:c.2+199_2+200delinsGC	ENSP00000477641.1:n.2+199_2+200delinsGC
ENST00000585851.1:c.291-1674_291-1673delinsGC	ENSP00000467912.1:n.291-1674_291-1673delinsGC
ENST00000586243.5:c.374+199_374+200delinsGC	ENSP00000467240.2:n.374+199_374+200delinsGC
ENST00000586358.5:n.197+199_197+200delinsGC
ENST00000589152.5:n.464+199_464+200delinsGC
ENST00000593219.5:c.*199+199_*199+200delinsGC	ENSP00000466610.1:n.*199+199_*199+200delinsGC
NM_000455.4:c.374+199_374+200delinsGC , LRG_319t1:c.374+199_374+200delinsGC	NP_000446.1:n.374+199_374+200delinsGC
XM_005259617.1:c.374+199_374+200delinsGC	XP_005259674.1:n.374+199_374+200delinsGC
XM_005259618.3:c.374+199_374+200delinsGC	XP_005259675.1:n.374+199_374+200delinsGC
XM_011528209.1:c.152+199_152+200delinsGC	XP_011526511.1:n.152+199_152+200delinsGC
XR_936204.1:n.999+199_999+200delinsGC
XM_005259617.3:c.374+199_374+200delinsGC	XP_005259674.1:n.374+199_374+200delinsGC
XM_011528209.2:c.152+199_152+200delinsGC	XP_011526511.1:n.152+199_152+200delinsGC
XR_001753738.2:n.999+199_999+200delinsGC
XR_001753739.1:n.999+199_999+200delinsGC
XR_001753740.2:n.999+199_999+200delinsGC
NM_000455.5:c.374+199_374+200delinsGC MANE Select	NP_000446.1:n.374+199_374+200delinsGC