Canonical Allele Identifier: CA2317593768

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226598G= , CM000681.2:g.1226598G=	GRCh38
NC_000019.9:g.1226597G= , CM000681.1:g.1226597G=	GRCh37
NC_000019.8:g.1177597G=	NCBI36
NG_007460.2:g.42192G= , LRG_319:g.42192G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1253G= MANE Select	NP_000446.1:p.Cys418=
ENST00000326873.12:c.1253G= MANE Select	ENSP00000324856.6:p.Cys418=
NM_000455.4:c.1253G= , LRG_319t1:c.1253G=	NP_000446.1:p.Cys418=
ENST00000326873.11:c.1253G=	ENSP00000324856.6:p.Cys418=
ENST00000585465.2:n.2986G=
ENST00000585465.3:c.*2854G=	ENSP00000490268.2:n.*2854G=
ENST00000585748.3:c.881G=	ENSP00000477641.2:p.Cys294=
ENST00000585851.2:c.1079G=	ENSP00000467912.2:p.Cys360=
ENST00000586243.5:c.1252G=	ENSP00000467240.2:p.Ala418=
ENST00000589152.5:n.1951G=
XM_005259617.1:c.1248G=	XP_005259674.1:p.Leu416=
XM_005259617.3:c.1248G=	XP_005259674.1:p.Leu416=
XM_011528209.1:c.1026G=	XP_011526511.1:p.Leu342=
XM_011528209.2:c.1026G=	XP_011526511.1:p.Leu342=
XR_001753738.2:n.2059G=
XR_001753740.2:n.2029G=