Canonical Allele Identifier: CA2580096068

Gene: STK11

Linked Data

• ClinVar Variation Id: 2452000
• ClinVar RCV Id: RCV003187696

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220449_1220450dup , CM000681.2:g.1220449_1220450dup	GRCh38
NC_000019.9:g.1220448_1220449dup , CM000681.1:g.1220448_1220449dup	GRCh37
NC_000019.8:g.1171448_1171449dup	NCBI36
NG_007460.2:g.36043_36044dup , LRG_319:g.36043_36044dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.541_542dup	ENSP00000490268.2:p.Asn181LysfsTer?
ENST00000585748.3:c.169_170dup	ENSP00000477641.2:p.Asn57LysfsTer?
ENST00000585851.2:c.367_368dup	ENSP00000467912.2:p.Asn123LysfsTer?
ENST00000326873.12:c.541_542dup MANE Select	ENSP00000324856.6:p.Asn181LysfsTer?
ENST00000652231.1:c.541_542dup	ENSP00000498804.1:p.Asn181LysfsTer?
ENST00000326873.11:c.541_542dup	ENSP00000324856.6:p.Asn181LysfsTer?
ENST00000585851.1:c.367_368dup	ENSP00000467912.1:p.Asn123LysfsTer?
ENST00000586243.5:c.541_542dup	ENSP00000467240.2:p.Asn181LysfsTer?
ENST00000586358.5:n.364_365dup
ENST00000589152.5:n.631_632dup
ENST00000591133.2:n.437_438dup
NM_000455.4:c.541_542dup , LRG_319t1:c.541_542dup	NP_000446.1:p.Asn181LysfsTer?
XM_005259617.1:c.541_542dup	XP_005259674.1:p.Asn181LysfsTer?
XM_005259618.3:c.541_542dup	XP_005259675.1:p.Asn181LysfsTer?
XM_011528209.1:c.319_320dup	XP_011526511.1:p.Asn107LysfsTer?
XR_936204.1:n.1166_1167dup
XM_005259617.3:c.541_542dup	XP_005259674.1:p.Asn181LysfsTer?
XM_011528209.2:c.319_320dup	XP_011526511.1:p.Asn107LysfsTer?
XR_001753738.2:n.1166_1167dup
XR_001753739.1:n.1166_1167dup
XR_001753740.2:n.1166_1167dup
NM_000455.5:c.541_542dup MANE Select	NP_000446.1:p.Asn181LysfsTer?