Canonical Allele Identifier: CA2317593797

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226627T= , CM000681.2:g.1226627T=	GRCh38
NC_000019.9:g.1226626T= , CM000681.1:g.1226626T=	GRCh37
NC_000019.8:g.1177626T=	NCBI36
NG_007460.2:g.42221T= , LRG_319:g.42221T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2883T=	ENSP00000490268.2:n.*2883T=
ENST00000585748.3:c.910T=	ENSP00000477641.2:p.Ser304=
ENST00000585851.2:c.1108T=	ENSP00000467912.2:p.Ser370=
ENST00000326873.12:c.1282T= MANE Select	ENSP00000324856.6:p.Ser428=
ENST00000326873.11:c.1282T=	ENSP00000324856.6:p.Ser428=
ENST00000585465.2:n.3015T=
ENST00000586243.5:c.1279T=	ENSP00000467240.2:p.Ser427=
ENST00000589152.5:n.1980T=
NM_000455.4:c.1282T= , LRG_319t1:c.1282T=	NP_000446.1:p.Ser428=
XM_005259617.1:c.1277T=	XP_005259674.1:p.Val426=
XM_011528209.1:c.1055T=	XP_011526511.1:p.Val352=
XM_005259617.3:c.1277T=	XP_005259674.1:p.Val426=
XM_011528209.2:c.1055T=	XP_011526511.1:p.Val352=
XR_001753738.2:n.2088T=
XR_001753740.2:n.2058T=
NM_000455.5:c.1282T= MANE Select	NP_000446.1:p.Ser428=