Canonical Allele Identifier: CA2317593676

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226490A= , CM000681.2:g.1226490A=	GRCh38
NC_000019.9:g.1226489A= , CM000681.1:g.1226489A=	GRCh37
NC_000019.8:g.1177489A=	NCBI36
NG_007460.2:g.42084A= , LRG_319:g.42084A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1145A= MANE Select	NP_000446.1:p.Gln382=
ENST00000326873.12:c.1145A= MANE Select	ENSP00000324856.6:p.Gln382=
NM_000455.4:c.1145A= , LRG_319t1:c.1145A=	NP_000446.1:p.Gln382=
ENST00000326873.11:c.1145A=	ENSP00000324856.6:p.Gln382=
ENST00000585465.2:n.2878A=
ENST00000585465.3:c.*2746A=	ENSP00000490268.2:n.*2746A=
ENST00000585748.3:c.773A=	ENSP00000477641.2:p.Gln258=
ENST00000585851.2:c.971A=	ENSP00000467912.2:p.Gln324=
ENST00000586243.5:c.1145A=	ENSP00000467240.2:p.Gln382=
ENST00000589152.5:n.1843A=
XM_005259617.1:c.1140A=	XP_005259674.1:p.Thr380=
XM_005259617.3:c.1140A=	XP_005259674.1:p.Thr380=
XM_011528209.1:c.918A=	XP_011526511.1:p.Thr306=
XM_011528209.2:c.918A=	XP_011526511.1:p.Thr306=
XR_001753738.2:n.1951A=
XR_001753740.2:n.1921A=