Canonical Allele Identifier: CA2695227892

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220389dup , CM000681.2:g.1220389dup	GRCh38
NC_000019.9:g.1220388dup , CM000681.1:g.1220388dup	GRCh37
NC_000019.8:g.1171388dup	NCBI36
NG_007460.2:g.35983dup , LRG_319:g.35983dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.481dup	ENSP00000490268.2:p.Ile161AsnfsTer2
ENST00000585748.3:c.109dup	ENSP00000477641.2:p.Ile37AsnfsTer2
ENST00000585851.2:c.307dup	ENSP00000467912.2:p.Ile103AsnfsTer2
ENST00000326873.12:c.481dup MANE Select	ENSP00000324856.6:p.Ile161AsnfsTer2
ENST00000652231.1:c.481dup	ENSP00000498804.1:p.Ile161AsnfsTer2
ENST00000326873.11:c.481dup	ENSP00000324856.6:p.Ile161AsnfsTer2
ENST00000585851.1:c.307dup	ENSP00000467912.1:p.Ile103AsnfsTer2
ENST00000586243.5:c.481dup	ENSP00000467240.2:p.Ile161AsnfsTer2
ENST00000586358.5:n.304dup
ENST00000589152.5:n.571dup
ENST00000591133.2:n.377dup
NM_000455.4:c.481dup , LRG_319t1:c.481dup	NP_000446.1:p.Ile161AsnfsTer2
XM_005259617.1:c.481dup	XP_005259674.1:p.Ile161AsnfsTer2
XM_005259618.3:c.481dup	XP_005259675.1:p.Ile161AsnfsTer2
XM_011528209.1:c.259dup	XP_011526511.1:p.Ile87AsnfsTer2
XR_936204.1:n.1106dup
XM_005259617.3:c.481dup	XP_005259674.1:p.Ile161AsnfsTer2
XM_011528209.2:c.259dup	XP_011526511.1:p.Ile87AsnfsTer2
XR_001753738.2:n.1106dup
XR_001753739.1:n.1106dup
XR_001753740.2:n.1106dup
NM_000455.5:c.481dup MANE Select	NP_000446.1:p.Ile161AsnfsTer2