Canonical Allele Identifier: CA2317593762

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226592A= , CM000681.2:g.1226592A=	GRCh38
NC_000019.9:g.1226591A= , CM000681.1:g.1226591A=	GRCh37
NC_000019.8:g.1177591A=	NCBI36
NG_007460.2:g.42186A= , LRG_319:g.42186A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1247A= MANE Select	NP_000446.1:p.Lys416=
ENST00000326873.12:c.1247A= MANE Select	ENSP00000324856.6:p.Lys416=
NM_000455.4:c.1247A= , LRG_319t1:c.1247A=	NP_000446.1:p.Lys416=
ENST00000326873.11:c.1247A=	ENSP00000324856.6:p.Lys416=
ENST00000585465.2:n.2980A=
ENST00000585465.3:c.*2848A=	ENSP00000490268.2:n.*2848A=
ENST00000585748.3:c.875A=	ENSP00000477641.2:p.Lys292=
ENST00000585851.2:c.1073A=	ENSP00000467912.2:p.Lys358=
ENST00000586243.5:c.1246A=	ENSP00000467240.2:p.Arg416=
ENST00000589152.5:n.1945A=
XM_005259617.1:c.1242A=	XP_005259674.1:p.Gln414=
XM_005259617.3:c.1242A=	XP_005259674.1:p.Gln414=
XM_011528209.1:c.1020A=	XP_011526511.1:p.Gln340=
XM_011528209.2:c.1020A=	XP_011526511.1:p.Gln340=
XR_001753738.2:n.2053A=
XR_001753740.2:n.2023A=