Canonical Allele Identifier: CA2582592912

Gene: STK11

Linked Data

• gnomAD v4: 19-1220459-T-TCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220464_1220466dup , CM000681.2:g.1220464_1220466dup	GRCh38
NC_000019.9:g.1220463_1220465dup , CM000681.1:g.1220463_1220465dup	GRCh37
NC_000019.8:g.1171463_1171465dup	NCBI36
NG_007460.2:g.36058_36060dup , LRG_319:g.36058_36060dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.556_558dup	ENSP00000490268.2:p.Thr186_Gly187insThr
ENST00000585748.3:c.184_186dup	ENSP00000477641.2:p.Thr62_Gly63insThr
ENST00000585851.2:c.382_384dup	ENSP00000467912.2:p.Thr128_Gly129insThr
ENST00000326873.12:c.556_558dup MANE Select	ENSP00000324856.6:p.Thr186_Gly187insThr
ENST00000652231.1:c.556_558dup	ENSP00000498804.1:p.Thr186_Gly187insThr
ENST00000326873.11:c.556_558dup	ENSP00000324856.6:p.Thr186_Gly187insThr
ENST00000585851.1:c.382_384dup	ENSP00000467912.1:p.Thr128_Gly129insThr
ENST00000586243.5:c.556_558dup	ENSP00000467240.2:p.Thr186_Gly187insThr
ENST00000586358.5:n.379_381dup
ENST00000589152.5:n.646_648dup
ENST00000591133.2:n.452_454dup
NM_000455.4:c.556_558dup , LRG_319t1:c.556_558dup	NP_000446.1:p.Thr186_Gly187insThr
XM_005259617.1:c.556_558dup	XP_005259674.1:p.Thr186_Gly187insThr
XM_005259618.3:c.556_558dup	XP_005259675.1:p.Thr186_Gly187insThr
XM_011528209.1:c.334_336dup	XP_011526511.1:p.Thr112_Gly113insThr
XR_936204.1:n.1181_1183dup
XM_005259617.3:c.556_558dup	XP_005259674.1:p.Thr186_Gly187insThr
XM_011528209.2:c.334_336dup	XP_011526511.1:p.Thr112_Gly113insThr
XR_001753738.2:n.1181_1183dup
XR_001753739.1:n.1181_1183dup
XR_001753740.2:n.1181_1183dup
NM_000455.5:c.556_558dup MANE Select	NP_000446.1:p.Thr186_Gly187insThr