Canonical Allele Identifier: CA645604074

Gene: STK11

Linked Data - Expert Curation

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220487_1220488delinsAT , CM000681.2:g.1220487_1220488delinsAT	GRCh38
NC_000019.9:g.1220486_1220487delinsAT , CM000681.1:g.1220486_1220487delinsAT	GRCh37
NC_000019.8:g.1171486_1171487delinsAT	NCBI36
NG_007460.2:g.36081_36082delinsAT , LRG_319:g.36081_36082delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.579_580delinsAT	ENSP00000490268.2:p.Asp194Tyr
ENST00000585748.3:c.207_208delinsAT	ENSP00000477641.2:p.Asp70Tyr
ENST00000585851.2:c.405_406delinsAT	ENSP00000467912.2:p.Asp136Tyr
ENST00000326873.12:c.579_580delinsAT MANE Select	ENSP00000324856.6:p.Asp194Tyr
ENST00000652231.1:c.579_580delinsAT	ENSP00000498804.1:p.Asp194Tyr
ENST00000326873.11:c.579_580delinsAT	ENSP00000324856.6:p.Asp194Tyr
ENST00000585851.1:c.405_406delinsAT	ENSP00000467912.1:p.Asp136Tyr
ENST00000586243.5:c.579_580delinsAT	ENSP00000467240.2:p.Asp194Tyr
ENST00000586358.5:n.402_403delinsAT
ENST00000589152.5:n.669_670delinsAT
ENST00000591133.2:n.475_476delinsAT
NM_000455.4:c.579_580delinsAT , LRG_319t1:c.579_580delinsAT	NP_000446.1:p.Asp194Tyr
XM_005259617.1:c.579_580delinsAT	XP_005259674.1:p.Asp194Tyr
XM_005259618.3:c.579_580delinsAT	XP_005259675.1:p.Asp194Tyr
XM_011528209.1:c.357_358delinsAT	XP_011526511.1:p.Asp120Tyr
XR_936204.1:n.1204_1205delinsAT
XM_005259617.3:c.579_580delinsAT	XP_005259674.1:p.Asp194Tyr
XM_011528209.2:c.357_358delinsAT	XP_011526511.1:p.Asp120Tyr
XR_001753738.2:n.1204_1205delinsAT
XR_001753739.1:n.1204_1205delinsAT
XR_001753740.2:n.1204_1205delinsAT
NM_000455.5:c.579_580delinsAT MANE Select	NP_000446.1:p.Asp194Tyr