Canonical Allele Identifier: CA16620744

Gene: STK11

Linked Data

• ClinVar Variation Id: 421459
• ClinVar RCV Id: RCV000480132 ; RCV000492438 ; RCV001809438
• dbSNP Id: rs775595174
• COSMIC: COSM20875
• MyVariant Identifiers: chr19:g.1218483G>T (hg19) ; chr19:g.1218484G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218484G>T , CM000681.2:g.1218484G>T	GRCh38
NC_000019.9:g.1218483G>T , CM000681.1:g.1218483G>T	GRCh37
NC_000019.8:g.1169483G>T	NCBI36
NG_007460.2:g.34078G>T , LRG_319:g.34078G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.358G>T	ENSP00000490268.2:p.Glu120Ter
ENST00000585748.3:c.-15G>T	ENSP00000477641.2:n.-15G>T
ENST00000585851.2:c.291-1889G>T	ENSP00000467912.2:n.291-1889G>T
ENST00000326873.12:c.358G>T MANE Select	ENSP00000324856.6:p.Glu120Ter
ENST00000652231.1:c.358G>T	ENSP00000498804.1:p.Glu120Ter
ENST00000326873.11:c.358G>T	ENSP00000324856.6:p.Glu120Ter
ENST00000585748.2:c.-15G>T	ENSP00000477641.1:n.-15G>T
ENST00000585851.1:c.291-1889G>T	ENSP00000467912.1:n.291-1889G>T
ENST00000586243.5:c.358G>T	ENSP00000467240.2:p.Glu120Ter
ENST00000586358.5:n.181G>T
ENST00000589152.5:n.448G>T
ENST00000593219.5:c.*183G>T	ENSP00000466610.1:n.*183G>T
NM_000455.4:c.358G>T , LRG_319t1:c.358G>T	NP_000446.1:p.Glu120Ter
XM_005259617.1:c.358G>T	XP_005259674.1:p.Glu120Ter
XM_005259618.3:c.358G>T	XP_005259675.1:p.Glu120Ter
XM_011528209.1:c.136G>T	XP_011526511.1:p.Glu46Ter
XR_936204.1:n.983G>T
XM_005259617.3:c.358G>T	XP_005259674.1:p.Glu120Ter
XM_011528209.2:c.136G>T	XP_011526511.1:p.Glu46Ter
XR_001753738.2:n.983G>T
XR_001753739.1:n.983G>T
XR_001753740.2:n.983G>T
NM_000455.5:c.358G>T MANE Select	NP_000446.1:p.Glu120Ter