Canonical Allele Identifier: CA2317581519

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206900_1206901delinsAC , CM000681.2:g.1206900_1206901delinsAC	GRCh38
NC_000019.9:g.1206899_1206900delinsAC , CM000681.1:g.1206899_1206900delinsAC	GRCh37
NC_000019.8:g.1157899_1157900delinsAC	NCBI36
NG_007460.2:g.22494_22495delinsAC , LRG_319:g.22494_22495delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-14_-13delinsAC	ENSP00000490268.2:n.-14_-13delinsAC
ENST00000585748.3:c.-82-11517_-82-11516delinsAC	ENSP00000477641.2:n.-82-11517_-82-11516delinsAC
ENST00000585851.2:c.-14_-13delinsAC	ENSP00000467912.2:n.-14_-13delinsAC
ENST00000326873.12:c.-14_-13delinsAC MANE Select	ENSP00000324856.6:n.-14_-13delinsAC
ENST00000652231.1:c.-14_-13delinsAC	ENSP00000498804.1:n.-14_-13delinsAC
ENST00000326873.11:c.-14_-13delinsAC	ENSP00000324856.6:n.-14_-13delinsAC
ENST00000585748.2:c.-82-11517_-82-11516delinsAC	ENSP00000477641.1:n.-82-11517_-82-11516delinsAC
ENST00000585851.1:c.-14_-13delinsAC	ENSP00000467912.1:n.-14_-13delinsAC
ENST00000586243.5:c.-14_-13delinsAC	ENSP00000467240.2:n.-14_-13delinsAC
ENST00000589152.5:n.77_78delinsAC
ENST00000593219.5:c.-14_-13delinsAC	ENSP00000466610.1:n.-14_-13delinsAC
NM_000455.4:c.-14_-13delinsAC , LRG_319t1:c.-14_-13delinsAC	NP_000446.1:n.-14_-13delinsAC
XM_005259617.1:c.-14_-13delinsAC	XP_005259674.1:n.-14_-13delinsAC
XM_005259618.3:c.-14_-13delinsAC	XP_005259675.1:n.-14_-13delinsAC
XM_011528209.1:c.-367_-366delinsAC	XP_011526511.1:n.-367_-366delinsAC
XR_936204.1:n.612_613delinsAC
XM_005259617.3:c.-14_-13delinsAC	XP_005259674.1:n.-14_-13delinsAC
XM_011528209.2:c.-367_-366delinsAC	XP_011526511.1:n.-367_-366delinsAC
XR_001753738.2:n.612_613delinsAC
XR_001753739.1:n.612_613delinsAC
XR_001753740.2:n.612_613delinsAC
NM_000455.5:c.-14_-13delinsAC MANE Select	NP_000446.1:n.-14_-13delinsAC