Canonical Allele Identifier: CA2317593758

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226585G= , CM000681.2:g.1226585G=	GRCh38
NC_000019.9:g.1226584G= , CM000681.1:g.1226584G=	GRCh37
NC_000019.8:g.1177584G=	NCBI36
NG_007460.2:g.42179G= , LRG_319:g.42179G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2841G=	ENSP00000490268.2:n.*2841G=
ENST00000585748.3:c.868G=	ENSP00000477641.2:p.Ala290=
ENST00000585851.2:c.1066G=	ENSP00000467912.2:p.Ala356=
ENST00000326873.12:c.1240G= MANE Select	ENSP00000324856.6:p.Ala414=
ENST00000326873.11:c.1240G=	ENSP00000324856.6:p.Ala414=
ENST00000585465.2:n.2973G=
ENST00000586243.5:c.1239G=	ENSP00000467240.2:p.Leu413=
ENST00000589152.5:n.1938G=
NM_000455.4:c.1240G= , LRG_319t1:c.1240G=	NP_000446.1:p.Ala414=
XM_005259617.1:c.1235G=	XP_005259674.1:p.Cys412=
XM_011528209.1:c.1013G=	XP_011526511.1:p.Cys338=
XM_005259617.3:c.1235G=	XP_005259674.1:p.Cys412=
XM_011528209.2:c.1013G=	XP_011526511.1:p.Cys338=
XR_001753738.2:n.2046G=
XR_001753740.2:n.2016G=
NM_000455.5:c.1240G= MANE Select	NP_000446.1:p.Ala414=