Canonical Allele Identifier: CA2813238262

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219693_1219694del , CM000681.2:g.1219693_1219694del	GRCh38
NC_000019.9:g.1219692_1219693del , CM000681.1:g.1219692_1219693del	GRCh37
NC_000019.8:g.1170692_1170693del	NCBI36
NG_007460.2:g.35287_35288del , LRG_319:g.35287_35288del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+280_464+281del	ENSP00000490268.2:n.464+280_464+281del
ENST00000585748.3:c.92+280_92+281del	ENSP00000477641.2:n.92+280_92+281del
ENST00000585851.2:c.291-680_291-679del	ENSP00000467912.2:n.291-680_291-679del
ENST00000326873.12:c.464+280_464+281del MANE Select	ENSP00000324856.6:n.464+280_464+281del
ENST00000652231.1:c.464+280_464+281del	ENSP00000498804.1:n.464+280_464+281del
ENST00000326873.11:c.464+280_464+281del	ENSP00000324856.6:n.464+280_464+281del
ENST00000585851.1:c.291-680_291-679del	ENSP00000467912.1:n.291-680_291-679del
ENST00000586243.5:c.464+280_464+281del	ENSP00000467240.2:n.464+280_464+281del
ENST00000586358.5:n.287+280_287+281del
ENST00000589152.5:n.554+280_554+281del
NM_000455.4:c.464+280_464+281del , LRG_319t1:c.464+280_464+281del	NP_000446.1:n.464+280_464+281del
XM_005259617.1:c.464+280_464+281del	XP_005259674.1:n.464+280_464+281del
XM_005259618.3:c.464+280_464+281del	XP_005259675.1:n.464+280_464+281del
XM_011528209.1:c.242+280_242+281del	XP_011526511.1:n.242+280_242+281del
XR_936204.1:n.1089+280_1089+281del
XM_005259617.3:c.464+280_464+281del	XP_005259674.1:n.464+280_464+281del
XM_011528209.2:c.242+280_242+281del	XP_011526511.1:n.242+280_242+281del
XR_001753738.2:n.1089+280_1089+281del
XR_001753739.1:n.1089+280_1089+281del
XR_001753740.2:n.1089+280_1089+281del
NM_000455.5:c.464+280_464+281del MANE Select	NP_000446.1:n.464+280_464+281del