Canonical Allele Identifier: CA2317593731

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226554A= , CM000681.2:g.1226554A=	GRCh38
NC_000019.9:g.1226553A= , CM000681.1:g.1226553A=	GRCh37
NC_000019.8:g.1177553A=	NCBI36
NG_007460.2:g.42148A= , LRG_319:g.42148A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2810A=	ENSP00000490268.2:n.*2810A=
ENST00000585748.3:c.837A=	ENSP00000477641.2:p.Lys279=
ENST00000585851.2:c.1035A=	ENSP00000467912.2:p.Lys345=
ENST00000326873.12:c.1209A= MANE Select	ENSP00000324856.6:p.Lys403=
ENST00000326873.11:c.1209A=	ENSP00000324856.6:p.Lys403=
ENST00000585465.2:n.2942A=
ENST00000586243.5:c.1209A=	ENSP00000467240.2:p.Lys403=
ENST00000589152.5:n.1907A=
NM_000455.4:c.1209A= , LRG_319t1:c.1209A=	NP_000446.1:p.Lys403=
XM_005259617.1:c.1204A=	XP_005259674.1:p.Ile402=
XM_011528209.1:c.982A=	XP_011526511.1:p.Ile328=
XM_005259617.3:c.1204A=	XP_005259674.1:p.Ile402=
XM_011528209.2:c.982A=	XP_011526511.1:p.Ile328=
XR_001753738.2:n.2015A=
XR_001753740.2:n.1985A=
NM_000455.5:c.1209A= MANE Select	NP_000446.1:p.Lys403=