Canonical Allele Identifier: CA2580096044

Gene: STK11

Linked Data

• ClinVar Variation Id: 1775237
• ClinVar RCV Id: RCV002405390 ; RCV004059120

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207069_1207070dup , CM000681.2:g.1207069_1207070dup	GRCh38
NC_000019.9:g.1207068_1207069dup , CM000681.1:g.1207068_1207069dup	GRCh37
NC_000019.8:g.1158068_1158069dup	NCBI36
NG_007460.2:g.22663_22664dup , LRG_319:g.22663_22664dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.156_157dup	ENSP00000490268.2:p.Asp53GlyfsTer12
ENST00000585748.3:c.-82-11348_-82-11347dup	ENSP00000477641.2:n.-82-11348_-82-11347dup
ENST00000585851.2:c.156_157dup	ENSP00000467912.2:p.Asp53GlyfsTer12
ENST00000326873.12:c.156_157dup MANE Select	ENSP00000324856.6:p.Asp53GlyfsTer12
ENST00000652231.1:c.156_157dup	ENSP00000498804.1:p.Asp53GlyfsTer12
ENST00000326873.11:c.156_157dup	ENSP00000324856.6:p.Asp53GlyfsTer12
ENST00000585748.2:c.-82-11348_-82-11347dup	ENSP00000477641.1:n.-82-11348_-82-11347dup
ENST00000585851.1:c.156_157dup	ENSP00000467912.1:p.Asp53GlyfsTer12
ENST00000586243.5:c.156_157dup	ENSP00000467240.2:p.Asp53GlyfsTer12
ENST00000589152.5:n.246_247dup
ENST00000593219.5:c.156_157dup	ENSP00000466610.1:p.Asp53GlyfsTer12
NM_000455.4:c.156_157dup , LRG_319t1:c.156_157dup	NP_000446.1:p.Asp53GlyfsTer12
XM_005259617.1:c.156_157dup	XP_005259674.1:p.Asp53GlyfsTer12
XM_005259618.3:c.156_157dup	XP_005259675.1:p.Asp53GlyfsTer12
XM_011528209.1:c.-198_-197dup	XP_011526511.1:n.-198_-197dup
XR_936204.1:n.781_782dup
XM_005259617.3:c.156_157dup	XP_005259674.1:p.Asp53GlyfsTer12
XM_011528209.2:c.-198_-197dup	XP_011526511.1:n.-198_-197dup
XR_001753738.2:n.781_782dup
XR_001753739.1:n.781_782dup
XR_001753740.2:n.781_782dup
NM_000455.5:c.156_157dup MANE Select	NP_000446.1:p.Asp53GlyfsTer12