Canonical Allele Identifier: CA2317581757

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207211_1207232delinsTGGCTTGCTGGGGTCGGGGCCG , CM000681.2:g.1207211_1207232delinsTGGCTTGCTGGGGTCGGGGCCG	GRCh38
NC_000019.9:g.1207210_1207231delinsTGGCTTGCTGGGGTCGGGGCCG , CM000681.1:g.1207210_1207231delinsTGGCTTGCTGGGGTCGGGGCCG	GRCh37
NC_000019.8:g.1158210_1158231delinsTGGCTTGCTGGGGTCGGGGCCG	NCBI36
NG_007460.2:g.22805_22826delinsTGGCTTGCTGGGGTCGGGGCCG , LRG_319:g.22805_22826delinsTGGCTTGCTGGGGTCGGGGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	ENSP00000490268.2:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
ENST00000585748.3:c.-82-11206_-82-11185delinsTGGCTTGCTGGGGTCGGGGCCG	ENSP00000477641.2:n.-82-11206_-82-11185delinsTGGCTTGCTGGGGTCG...
ENST00000585851.2:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	ENSP00000467912.2:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
ENST00000326873.12:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG MANE Select	ENSP00000324856.6:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
ENST00000652231.1:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	ENSP00000498804.1:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
ENST00000326873.11:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	ENSP00000324856.6:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
ENST00000585748.2:c.-82-11206_-82-11185delinsTGGCTTGCTGGGGTCGGGGCCG	ENSP00000477641.1:n.-82-11206_-82-11185delinsTGGCTTGCTGGGGTCG...
ENST00000585851.1:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	ENSP00000467912.1:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
ENST00000586243.5:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	ENSP00000467240.2:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
ENST00000586358.5:n.113+8_113+29delinsTGGCTTGCTGGGGTCGGGGCCG
ENST00000589152.5:n.380+8_380+29delinsTGGCTTGCTGGGGTCGGGGCCG
ENST00000593219.5:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	ENSP00000466610.1:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
NM_000455.4:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG , LRG_319t1:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	NP_000446.1:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
XM_005259617.1:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	XP_005259674.1:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
XM_005259618.3:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	XP_005259675.1:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
XM_011528209.1:c.-64+8_-64+29delinsTGGCTTGCTGGGGTCGGGGCCG	XP_011526511.1:n.-64+8_-64+29delinsTGGCTTGCTGGGGTCGGGGCCG
XR_936204.1:n.915+8_915+29delinsTGGCTTGCTGGGGTCGGGGCCG
XM_005259617.3:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG	XP_005259674.1:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG
XM_011528209.2:c.-64+8_-64+29delinsTGGCTTGCTGGGGTCGGGGCCG	XP_011526511.1:n.-64+8_-64+29delinsTGGCTTGCTGGGGTCGGGGCCG
XR_001753738.2:n.915+8_915+29delinsTGGCTTGCTGGGGTCGGGGCCG
XR_001753739.1:n.915+8_915+29delinsTGGCTTGCTGGGGTCGGGGCCG
XR_001753740.2:n.915+8_915+29delinsTGGCTTGCTGGGGTCGGGGCCG
NM_000455.5:c.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG MANE Select	NP_000446.1:n.290+8_290+29delinsTGGCTTGCTGGGGTCGGGGCCG