Canonical Allele Identifier: CA2317593687

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226505C= , CM000681.2:g.1226505C=	GRCh38
NC_000019.9:g.1226504C= , CM000681.1:g.1226504C=	GRCh37
NC_000019.8:g.1177504C=	NCBI36
NG_007460.2:g.42099C= , LRG_319:g.42099C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2761C=	ENSP00000490268.2:n.*2761C=
ENST00000585748.3:c.788C=	ENSP00000477641.2:p.Pro263=
ENST00000585851.2:c.986C=	ENSP00000467912.2:p.Pro329=
ENST00000326873.12:c.1160C= MANE Select	ENSP00000324856.6:p.Pro387=
ENST00000326873.11:c.1160C=	ENSP00000324856.6:p.Pro387=
ENST00000585465.2:n.2893C=
ENST00000586243.5:c.1160C=	ENSP00000467240.2:p.Pro387=
ENST00000589152.5:n.1858C=
NM_000455.4:c.1160C= , LRG_319t1:c.1160C=	NP_000446.1:p.Pro387=
XM_005259617.1:c.1155C=	XP_005259674.1:p.Pro385=
XM_011528209.1:c.933C=	XP_011526511.1:p.Pro311=
XM_005259617.3:c.1155C=	XP_005259674.1:p.Pro385=
XM_011528209.2:c.933C=	XP_011526511.1:p.Pro311=
XR_001753738.2:n.1966C=
XR_001753740.2:n.1936C=
NM_000455.5:c.1160C= MANE Select	NP_000446.1:p.Pro387=