Canonical Allele Identifier: CA2317591437

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222985_1222995delinsCTGGTTCCGGA , CM000681.2:g.1222985_1222995delinsCTGGTTCCGGA	GRCh38
NC_000019.9:g.1222984_1222994delinsCTGGTTCCGGA , CM000681.1:g.1222984_1222994delinsCTGGTTCCGGA	GRCh37
NC_000019.8:g.1173984_1173994delinsCTGGTTCCGGA	NCBI36
NG_007460.2:g.38579_38589delinsCTGGTTCCGGA , LRG_319:g.38579_38589delinsCTGGTTCCGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.921_931delinsCTGGTTCCGGA	ENSP00000490268.2:p.Ser307=
ENST00000585748.3:c.549_559delinsCTGGTTCCGGA	ENSP00000477641.2:p.Ser183=
ENST00000585851.2:c.747_757delinsCTGGTTCCGGA	ENSP00000467912.2:p.Ser249=
ENST00000326873.12:c.921_931delinsCTGGTTCCGGA MANE Select	ENSP00000324856.6:p.Ser307=
ENST00000652231.1:c.921_931delinsCTGGTTCCGGA	ENSP00000498804.1:p.Ser307=
ENST00000326873.11:c.921_931delinsCTGGTTCCGGA	ENSP00000324856.6:p.Ser307=
ENST00000586243.5:c.921_931delinsCTGGTTCCGGA	ENSP00000467240.2:p.Ser307=
ENST00000589152.5:n.1619_1629delinsCTGGTTCCGGA
ENST00000591133.2:n.892_902delinsCTGGTTCCGGA
NM_000455.4:c.921_931delinsCTGGTTCCGGA , LRG_319t1:c.921_931delinsCTGGTTCCGGA	NP_000446.1:p.Ser307=
XM_005259617.1:c.921_931delinsCTGGTTCCGGA	XP_005259674.1:p.Ser307=
XM_005259618.3:c.921_931delinsCTGGTTCCGGA	XP_005259675.1:p.Ser307=
XM_011528209.1:c.699_709delinsCTGGTTCCGGA	XP_011526511.1:p.Ser233=
XR_936204.1:n.1697_1707delinsCTGGTTCCGGA
XM_005259617.3:c.921_931delinsCTGGTTCCGGA	XP_005259674.1:p.Ser307=
XM_011528209.2:c.699_709delinsCTGGTTCCGGA	XP_011526511.1:p.Ser233=
XR_001753738.2:n.1727_1737delinsCTGGTTCCGGA
XR_001753739.1:n.1727_1737delinsCTGGTTCCGGA
XR_001753740.2:n.1697_1707delinsCTGGTTCCGGA
NM_000455.5:c.921_931delinsCTGGTTCCGGA MANE Select	NP_000446.1:p.Ser307=