Canonical Allele Identifier: CA915951597

Gene: STK11

Linked Data

• ClinVar Variation Id: 823105
• ClinVar RCV Id: RCV001019033
• dbSNP Id: rs1599929258

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222986_1222995delinsCC , CM000681.2:g.1222986_1222995delinsCC	GRCh38
NC_000019.9:g.1222985_1222994delinsCC , CM000681.1:g.1222985_1222994delinsCC	GRCh37
NC_000019.8:g.1173985_1173994delinsCC	NCBI36
NG_007460.2:g.38580_38589delinsCC , LRG_319:g.38580_38589delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.922_931delinsCC	ENSP00000490268.2:p.Trp308ProfsTer7
ENST00000585748.3:c.550_559delinsCC	ENSP00000477641.2:p.Trp184ProfsTer7
ENST00000585851.2:c.748_757delinsCC	ENSP00000467912.2:p.Trp250ProfsTer7
ENST00000326873.12:c.922_931delinsCC MANE Select	ENSP00000324856.6:p.Trp308ProfsTer7
ENST00000652231.1:c.922_931delinsCC	ENSP00000498804.1:p.Trp308ProfsTer7
ENST00000326873.11:c.922_931delinsCC	ENSP00000324856.6:p.Trp308ProfsTer7
ENST00000586243.5:c.922_931delinsCC	ENSP00000467240.2:p.Trp308ProfsTer7
ENST00000589152.5:n.1620_1629delinsCC
ENST00000591133.2:n.893_902delinsCC
NM_000455.4:c.922_931delinsCC , LRG_319t1:c.922_931delinsCC	NP_000446.1:p.Trp308ProfsTer7
XM_005259617.1:c.922_931delinsCC	XP_005259674.1:p.Trp308ProfsTer7
XM_005259618.3:c.922_931delinsCC	XP_005259675.1:p.Trp308ProfsTer7
XM_011528209.1:c.700_709delinsCC	XP_011526511.1:p.Trp234ProfsTer7
XR_936204.1:n.1698_1707delinsCC
XM_005259617.3:c.922_931delinsCC	XP_005259674.1:p.Trp308ProfsTer7
XM_011528209.2:c.700_709delinsCC	XP_011526511.1:p.Trp234ProfsTer7
XR_001753738.2:n.1728_1737delinsCC
XR_001753739.1:n.1728_1737delinsCC
XR_001753740.2:n.1698_1707delinsCC
NM_000455.5:c.922_931delinsCC MANE Select	NP_000446.1:p.Trp308ProfsTer7