Canonical Allele Identifier: CA2317590283

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221195_1221197delinsCCT , CM000681.2:g.1221195_1221197delinsCCT	GRCh38
NC_000019.9:g.1221194_1221196delinsCCT , CM000681.1:g.1221194_1221196delinsCCT	GRCh37
NC_000019.8:g.1172194_1172196delinsCCT	NCBI36
NG_007460.2:g.36789_36791delinsCCT , LRG_319:g.36789_36791delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.735-18_735-16delinsCCT	ENSP00000490268.2:n.735-18_735-16delinsCCT
ENST00000585748.3:c.363-18_363-16delinsCCT	ENSP00000477641.2:n.363-18_363-16delinsCCT
ENST00000585851.2:c.561-18_561-16delinsCCT	ENSP00000467912.2:n.561-18_561-16delinsCCT
ENST00000326873.12:c.735-18_735-16delinsCCT MANE Select	ENSP00000324856.6:n.735-18_735-16delinsCCT
ENST00000652231.1:c.735-18_735-16delinsCCT	ENSP00000498804.1:n.735-18_735-16delinsCCT
ENST00000326873.11:c.735-18_735-16delinsCCT	ENSP00000324856.6:n.735-18_735-16delinsCCT
ENST00000586243.5:c.735-18_735-16delinsCCT	ENSP00000467240.2:n.735-18_735-16delinsCCT
ENST00000586358.5:n.633-18_633-16delinsCCT
ENST00000589152.5:n.825-18_825-16delinsCCT
ENST00000591133.2:n.706-18_706-16delinsCCT
NM_000455.4:c.735-18_735-16delinsCCT , LRG_319t1:c.735-18_735-16delinsCCT	NP_000446.1:n.735-18_735-16delinsCCT
XM_005259617.1:c.735-18_735-16delinsCCT	XP_005259674.1:n.735-18_735-16delinsCCT
XM_005259618.3:c.735-18_735-16delinsCCT	XP_005259675.1:n.735-18_735-16delinsCCT
XM_011528209.1:c.513-18_513-16delinsCCT	XP_011526511.1:n.513-18_513-16delinsCCT
XR_936204.1:n.1360-18_1360-16delinsCCT
XM_005259617.3:c.735-18_735-16delinsCCT	XP_005259674.1:n.735-18_735-16delinsCCT
XM_011528209.2:c.513-18_513-16delinsCCT	XP_011526511.1:n.513-18_513-16delinsCCT
XR_001753738.2:n.1360-18_1360-16delinsCCT
XR_001753739.1:n.1360-18_1360-16delinsCCT
XR_001753740.2:n.1360-18_1360-16delinsCCT
NM_000455.5:c.735-18_735-16delinsCCT MANE Select	NP_000446.1:n.735-18_735-16delinsCCT