Canonical Allele Identifier: CA2317593670

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226484A= , CM000681.2:g.1226484A=	GRCh38
NC_000019.9:g.1226483A= , CM000681.1:g.1226483A=	GRCh37
NC_000019.8:g.1177483A=	NCBI36
NG_007460.2:g.42078A= , LRG_319:g.42078A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2740A=	ENSP00000490268.2:n.*2740A=
ENST00000585748.3:c.767A=	ENSP00000477641.2:p.Asn256=
ENST00000585851.2:c.965A=	ENSP00000467912.2:p.Asn322=
ENST00000326873.12:c.1139A= MANE Select	ENSP00000324856.6:p.Asn380=
ENST00000326873.11:c.1139A=	ENSP00000324856.6:p.Asn380=
ENST00000585465.2:n.2872A=
ENST00000586243.5:c.1139A=	ENSP00000467240.2:p.Asn380=
ENST00000589152.5:n.1837A=
NM_000455.4:c.1139A= , LRG_319t1:c.1139A=	NP_000446.1:p.Asn380=
XM_005259617.1:c.1134A=	XP_005259674.1:p.Gln378=
XM_011528209.1:c.912A=	XP_011526511.1:p.Gln304=
XM_005259617.3:c.1134A=	XP_005259674.1:p.Gln378=
XM_011528209.2:c.912A=	XP_011526511.1:p.Gln304=
XR_001753738.2:n.1945A=
XR_001753740.2:n.1915A=
NM_000455.5:c.1139A= MANE Select	NP_000446.1:p.Asn380=