Canonical Allele Identifier: CA658684198

Gene: STK11

Linked Data

• ClinVar Variation Id: 492531
• ClinVar RCV Id: RCV000581154

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219422_1219426delinsCCCGC , CM000681.2:g.1219422_1219426delinsCCCGC	GRCh38
NC_000019.9:g.1219421_1219425delinsCCCGC , CM000681.1:g.1219421_1219425delinsCCCGC	GRCh37
NC_000019.8:g.1170421_1170425delinsCCCGC	NCBI36
NG_007460.2:g.35016_35020delinsCCCGC , LRG_319:g.35016_35020delinsCCCGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.464+9_464+13delinsCCCGC	ENSP00000490268.2:n.464+9_464+13delinsCCC...
ENST00000585748.3:c.92+9_92+13delinsCCCGC	ENSP00000477641.2:n.92+9_92+13delinsCCCGC...
ENST00000585851.2:c.291-951_291-947delinsCCCGC	ENSP00000467912.2:n.291-951_291-947delins...
ENST00000326873.12:c.464+9_464+13delinsCCCGC MANE Select	ENSP00000324856.6:n.464+9_464+13delinsCCC...
ENST00000652231.1:c.464+9_464+13delinsCCCGC	ENSP00000498804.1:n.464+9_464+13delinsCCC...
ENST00000326873.11:c.464+9_464+13delinsCCCGC	ENSP00000324856.6:n.464+9_464+13delinsCCC...
ENST00000585851.1:c.291-951_291-947delinsCCCGC	ENSP00000467912.1:n.291-951_291-947delins...
ENST00000586243.5:c.464+9_464+13delinsCCCGC	ENSP00000467240.2:n.464+9_464+13delinsCCC...
ENST00000586358.5:n.287+9_287+13delinsCCCGC
ENST00000589152.5:n.554+9_554+13delinsCCCGC
NM_000455.4:c.464+9_464+13delinsCCCGC , LRG_319t1:c.464+9_464+13delinsCCCGC	NP_000446.1:n.464+9_464+13delinsCCCGC
XM_005259617.1:c.464+9_464+13delinsCCCGC	XP_005259674.1:n.464+9_464+13delinsCCCGC
XM_005259618.3:c.464+9_464+13delinsCCCGC	XP_005259675.1:n.464+9_464+13delinsCCCGC
XM_011528209.1:c.242+9_242+13delinsCCCGC	XP_011526511.1:n.242+9_242+13delinsCCCGC
XR_936204.1:n.1089+9_1089+13delinsCCCGC
XM_005259617.3:c.464+9_464+13delinsCCCGC	XP_005259674.1:n.464+9_464+13delinsCCCGC
XM_011528209.2:c.242+9_242+13delinsCCCGC	XP_011526511.1:n.242+9_242+13delinsCCCGC
XR_001753738.2:n.1089+9_1089+13delinsCCCGC
XR_001753739.1:n.1089+9_1089+13delinsCCCGC
XR_001753740.2:n.1089+9_1089+13delinsCCCGC
NM_000455.5:c.464+9_464+13delinsCCCGC MANE Select	NP_000446.1:n.464+9_464+13delinsCCCGC