Canonical Allele Identifier: CA915951598

Gene: STK11

Linked Data

• ClinVar Variation Id: 801287
• ClinVar RCV Id: RCV000986040
• dbSNP Id: rs1599929264

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222994del , CM000681.2:g.1222994del	GRCh38
NC_000019.9:g.1222993del , CM000681.1:g.1222993del	GRCh37
NC_000019.8:g.1173993del	NCBI36
NG_007460.2:g.38588del , LRG_319:g.38588del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.930del	ENSP00000490268.2:p.Lys311ArgfsTer25
ENST00000585748.3:c.558del	ENSP00000477641.2:p.Lys187ArgfsTer25
ENST00000585851.2:c.756del	ENSP00000467912.2:p.Lys253ArgfsTer25
ENST00000326873.12:c.930del MANE Select	ENSP00000324856.6:p.Lys311ArgfsTer25
ENST00000652231.1:c.930del	ENSP00000498804.1:p.Lys311ArgfsTer25
ENST00000326873.11:c.930del	ENSP00000324856.6:p.Lys311ArgfsTer25
ENST00000586243.5:c.930del	ENSP00000467240.2:p.Lys311ArgfsTer25
ENST00000589152.5:n.1628del
ENST00000591133.2:n.901del
NM_000455.4:c.930del , LRG_319t1:c.930del	NP_000446.1:p.Lys311ArgfsTer25
XM_005259617.1:c.930del	XP_005259674.1:p.Lys311ArgfsTer25
XM_005259618.3:c.930del	XP_005259675.1:p.Lys311ArgfsTer25
XM_011528209.1:c.708del	XP_011526511.1:p.Lys237ArgfsTer25
XR_936204.1:n.1706del
XM_005259617.3:c.930del	XP_005259674.1:p.Lys311ArgfsTer25
XM_011528209.2:c.708del	XP_011526511.1:p.Lys237ArgfsTer25
XR_001753738.2:n.1736del
XR_001753739.1:n.1736del
XR_001753740.2:n.1706del
NM_000455.5:c.930del MANE Select	NP_000446.1:p.Lys311ArgfsTer25