Canonical Allele Identifier: CA2576546266

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207279_1207282del , CM000681.2:g.1207279_1207282del	GRCh38
NC_000019.9:g.1207278_1207281del , CM000681.1:g.1207278_1207281del	GRCh37
NC_000019.8:g.1158278_1158281del	NCBI36
NG_007460.2:g.22873_22876del , LRG_319:g.22873_22876del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+76_290+79del	ENSP00000490268.2:n.290+76_290+79del
ENST00000585748.3:c.-82-11138_-82-11135del	ENSP00000477641.2:n.-82-11138_-82-11135del
ENST00000585851.2:c.290+76_290+79del	ENSP00000467912.2:n.290+76_290+79del
ENST00000326873.12:c.290+76_290+79del MANE Select	ENSP00000324856.6:n.290+76_290+79del
ENST00000652231.1:c.290+76_290+79del	ENSP00000498804.1:n.290+76_290+79del
ENST00000326873.11:c.290+76_290+79del	ENSP00000324856.6:n.290+76_290+79del
ENST00000585748.2:c.-82-11138_-82-11135del	ENSP00000477641.1:n.-82-11138_-82-11135del
ENST00000585851.1:c.290+76_290+79del	ENSP00000467912.1:n.290+76_290+79del
ENST00000586243.5:c.290+76_290+79del	ENSP00000467240.2:n.290+76_290+79del
ENST00000586358.5:n.113+76_113+79del
ENST00000589152.5:n.380+76_380+79del
ENST00000593219.5:c.290+76_290+79del	ENSP00000466610.1:n.290+76_290+79del
NM_000455.4:c.290+76_290+79del , LRG_319t1:c.290+76_290+79del	NP_000446.1:n.290+76_290+79del
XM_005259617.1:c.290+76_290+79del	XP_005259674.1:n.290+76_290+79del
XM_005259618.3:c.290+76_290+79del	XP_005259675.1:n.290+76_290+79del
XM_011528209.1:c.-64+76_-64+79del	XP_011526511.1:n.-64+76_-64+79del
XR_936204.1:n.915+76_915+79del
XM_005259617.3:c.290+76_290+79del	XP_005259674.1:n.290+76_290+79del
XM_011528209.2:c.-64+76_-64+79del	XP_011526511.1:n.-64+76_-64+79del
XR_001753738.2:n.915+76_915+79del
XR_001753739.1:n.915+76_915+79del
XR_001753740.2:n.915+76_915+79del
NM_000455.5:c.290+76_290+79del MANE Select	NP_000446.1:n.290+76_290+79del