Canonical Allele Identifier: CA913189006

Gene: STK11

Linked Data

• ClinVar Variation Id: 924453
• ClinVar RCV Id: RCV001185810
• dbSNP Id: rs2080824794

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226656_1226657delinsTA , CM000681.2:g.1226656_1226657delinsTA	GRCh38
NC_000019.9:g.1226655_1226656delinsTA , CM000681.1:g.1226655_1226656delinsTA	GRCh37
NC_000019.8:g.1177655_1177656delinsTA	NCBI36
NG_007460.2:g.42250_42251delinsTA , LRG_319:g.42250_42251delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2912_*2913delinsTA	ENSP00000490268.2:n.*2912_*2913delinsTA
ENST00000585748.3:c.*9_*10delinsTA	ENSP00000477641.2:n.*9_*10delinsTA
ENST00000585851.2:c.*9_*10delinsTA	ENSP00000467912.2:n.*9_*10delinsTA
ENST00000326873.12:c.*9_*10delinsTA MANE Select	ENSP00000324856.6:n.*9_*10delinsTA
ENST00000326873.11:c.*9_*10delinsTA	ENSP00000324856.6:n.*9_*10delinsTA
ENST00000585465.2:n.3044_3045delinsTA
ENST00000586243.5:c.*9_*10delinsTA	ENSP00000467240.2:n.*9_*10delinsTA
ENST00000589152.5:n.2009_2010delinsTA
NM_000455.4:c.*9_*10delinsTA , LRG_319t1:c.*9_*10delinsTA	NP_000446.1:n.*9_*10delinsTA
XM_005259617.1:c.1306_1307delinsTA	XP_005259674.1:p.Ala436Tyr
XM_011528209.1:c.1084_1085delinsTA	XP_011526511.1:p.Ala362Tyr
XM_005259617.3:c.1306_1307delinsTA	XP_005259674.1:p.Ala436Tyr
XM_011528209.2:c.1084_1085delinsTA	XP_011526511.1:p.Ala362Tyr
XR_001753738.2:n.2117_2118delinsTA
XR_001753740.2:n.2087_2088delinsTA
NM_000455.5:c.*9_*10delinsTA MANE Select	NP_000446.1:n.*9_*10delinsTA