Canonical Allele Identifier: CA2317593785

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226611C= , CM000681.2:g.1226611C=	GRCh38
NC_000019.9:g.1226610C= , CM000681.1:g.1226610C=	GRCh37
NC_000019.8:g.1177610C=	NCBI36
NG_007460.2:g.42205C= , LRG_319:g.42205C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2867C=	ENSP00000490268.2:n.*2867C=
ENST00000585748.3:c.894C=	ENSP00000477641.2:p.Ser298=
ENST00000585851.2:c.1092C=	ENSP00000467912.2:p.Ser364=
ENST00000326873.12:c.1266C= MANE Select	ENSP00000324856.6:p.Ser422=
ENST00000326873.11:c.1266C=	ENSP00000324856.6:p.Ser422=
ENST00000585465.2:n.2999C=
ENST00000586243.5:c.1263C=	ENSP00000467240.2:p.Ser421=
ENST00000589152.5:n.1964C=
NM_000455.4:c.1266C= , LRG_319t1:c.1266C=	NP_000446.1:p.Ser422=
XM_005259617.1:c.1261C=	XP_005259674.1:p.Gln421=
XM_011528209.1:c.1039C=	XP_011526511.1:p.Gln347=
XM_005259617.3:c.1261C=	XP_005259674.1:p.Gln421=
XM_011528209.2:c.1039C=	XP_011526511.1:p.Gln347=
XR_001753738.2:n.2072C=
XR_001753740.2:n.2042C=
NM_000455.5:c.1266C= MANE Select	NP_000446.1:p.Ser422=