Canonical Allele Identifier: CA2695227963

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221281_1221282delinsC , CM000681.2:g.1221281_1221282delinsC	GRCh38
NC_000019.9:g.1221280_1221281delinsC , CM000681.1:g.1221280_1221281delinsC	GRCh37
NC_000019.8:g.1172280_1172281delinsC	NCBI36
NG_007460.2:g.36875_36876delinsC , LRG_319:g.36875_36876delinsC

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.803_804delinsC	ENSP00000490268.2:p.Gly268AlafsTer19
ENST00000585748.3:c.431_432delinsC	ENSP00000477641.2:p.Gly144AlafsTer19
ENST00000585851.2:c.629_630delinsC	ENSP00000467912.2:p.Gly210AlafsTer19
ENST00000326873.12:c.803_804delinsC MANE Select	ENSP00000324856.6:p.Gly268AlafsTer19
ENST00000652231.1:c.803_804delinsC	ENSP00000498804.1:p.Gly268AlafsTer19
ENST00000326873.11:c.803_804delinsC	ENSP00000324856.6:p.Gly268AlafsTer19
ENST00000586243.5:c.803_804delinsC	ENSP00000467240.2:p.Gly268AlafsTer19
ENST00000586358.5:n.701_702delinsC
ENST00000589152.5:n.893_894delinsC
ENST00000591133.2:n.774_775delinsC
NM_000455.4:c.803_804delinsC , LRG_319t1:c.803_804delinsC	NP_000446.1:p.Gly268AlafsTer19
XM_005259617.1:c.803_804delinsC	XP_005259674.1:p.Gly268AlafsTer19
XM_005259618.3:c.803_804delinsC	XP_005259675.1:p.Gly268AlafsTer19
XM_011528209.1:c.581_582delinsC	XP_011526511.1:p.Gly194AlafsTer19
XR_936204.1:n.1428_1429delinsC
XM_005259617.3:c.803_804delinsC	XP_005259674.1:p.Gly268AlafsTer19
XM_011528209.2:c.581_582delinsC	XP_011526511.1:p.Gly194AlafsTer19
XR_001753738.2:n.1428_1429delinsC
XR_001753739.1:n.1428_1429delinsC
XR_001753740.2:n.1428_1429delinsC
NM_000455.5:c.803_804delinsC MANE Select	NP_000446.1:p.Gly268AlafsTer19