Canonical Allele Identifier: CA2317593754

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226581C= , CM000681.2:g.1226581C=	GRCh38
NC_000019.9:g.1226580C= , CM000681.1:g.1226580C=	GRCh37
NC_000019.8:g.1177580C=	NCBI36
NG_007460.2:g.42175C= , LRG_319:g.42175C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2837C=	ENSP00000490268.2:n.*2837C=
ENST00000585748.3:c.864C=	ENSP00000477641.2:p.Asn288=
ENST00000585851.2:c.1062C=	ENSP00000467912.2:p.Asn354=
ENST00000326873.12:c.1236C= MANE Select	ENSP00000324856.6:p.Asn412=
ENST00000326873.11:c.1236C=	ENSP00000324856.6:p.Asn412=
ENST00000585465.2:n.2969C=
ENST00000586243.5:c.1235C=	ENSP00000467240.2:p.Thr412=
ENST00000589152.5:n.1934C=
NM_000455.4:c.1236C= , LRG_319t1:c.1236C=	NP_000446.1:p.Asn412=
XM_005259617.1:c.1231C=	XP_005259674.1:p.Pro411=
XM_011528209.1:c.1009C=	XP_011526511.1:p.Pro337=
XM_005259617.3:c.1231C=	XP_005259674.1:p.Pro411=
XM_011528209.2:c.1009C=	XP_011526511.1:p.Pro337=
XR_001753738.2:n.2042C=
XR_001753740.2:n.2012C=
NM_000455.5:c.1236C= MANE Select	NP_000446.1:p.Asn412=