Canonical Allele Identifier: CA2317591514

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223077T= , CM000681.2:g.1223077T=	GRCh38
NC_000019.9:g.1223076T= , CM000681.1:g.1223076T=	GRCh37
NC_000019.8:g.1174076T=	NCBI36
NG_007460.2:g.38671T= , LRG_319:g.38671T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1013T=	ENSP00000490268.2:p.Val338=
ENST00000585748.3:c.641T=	ENSP00000477641.2:p.Val214=
ENST00000585851.2:c.839T=	ENSP00000467912.2:p.Val280=
ENST00000326873.12:c.1013T= MANE Select	ENSP00000324856.6:p.Val338=
ENST00000652231.1:c.1013T=	ENSP00000498804.1:p.Val338=
ENST00000326873.11:c.1013T=	ENSP00000324856.6:p.Val338=
ENST00000586243.5:c.1013T=	ENSP00000467240.2:p.Val338=
ENST00000589152.5:n.1711T=
ENST00000591133.2:n.984T=
NM_000455.4:c.1013T= , LRG_319t1:c.1013T=	NP_000446.1:p.Val338=
XM_005259617.1:c.1013T=	XP_005259674.1:p.Val338=
XM_005259618.3:c.1013T=	XP_005259675.1:p.Val338=
XM_011528209.1:c.791T=	XP_011526511.1:p.Val264=
XR_936204.1:n.1789T=
XM_005259617.3:c.1013T=	XP_005259674.1:p.Val338=
XM_011528209.2:c.791T=	XP_011526511.1:p.Val264=
XR_001753738.2:n.1819T=
XR_001753739.1:n.1819T=
XR_001753740.2:n.1789T=
NM_000455.5:c.1013T= MANE Select	NP_000446.1:p.Val338=