Canonical Allele Identifier: CA2317593787

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226614G= , CM000681.2:g.1226614G=	GRCh38
NC_000019.9:g.1226613G= , CM000681.1:g.1226613G=	GRCh37
NC_000019.8:g.1177613G=	NCBI36
NG_007460.2:g.42208G= , LRG_319:g.42208G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2870G=	ENSP00000490268.2:n.*2870G=
ENST00000585748.3:c.897G=	ENSP00000477641.2:p.Lys299=
ENST00000585851.2:c.1095G=	ENSP00000467912.2:p.Lys365=
ENST00000326873.12:c.1269G= MANE Select	ENSP00000324856.6:p.Lys423=
ENST00000326873.11:c.1269G=	ENSP00000324856.6:p.Lys423=
ENST00000585465.2:n.3002G=
ENST00000586243.5:c.1266G=	ENSP00000467240.2:p.Lys422=
ENST00000589152.5:n.1967G=
NM_000455.4:c.1269G= , LRG_319t1:c.1269G=	NP_000446.1:p.Lys423=
XM_005259617.1:c.1264G=	XP_005259674.1:p.Asp422=
XM_011528209.1:c.1042G=	XP_011526511.1:p.Asp348=
XM_005259617.3:c.1264G=	XP_005259674.1:p.Asp422=
XM_011528209.2:c.1042G=	XP_011526511.1:p.Asp348=
XR_001753738.2:n.2075G=
XR_001753740.2:n.2045G=
NM_000455.5:c.1269G= MANE Select	NP_000446.1:p.Lys423=