Canonical Allele Identifier: CA402947913

Gene: STK11

Linked Data

• ClinVar Variation Id: 428761
• ClinVar RCV Id: RCV000492251 ; RCV001856951
• dbSNP Id: rs1131690925
• COSMIC: COSM380443 ; COSM5224269
• MyVariant Identifiers: chr19:g.1218492C>T (hg19) ; chr19:g.1218493C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218493C>T , CM000681.2:g.1218493C>T	GRCh38
NC_000019.9:g.1218492C>T , CM000681.1:g.1218492C>T	GRCh37
NC_000019.8:g.1169492C>T	NCBI36
NG_007460.2:g.34087C>T , LRG_319:g.34087C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.367C>T	ENSP00000490268.2:p.Gln123Ter
ENST00000585748.3:c.-6C>T	ENSP00000477641.2:n.-6C>T
ENST00000585851.2:c.291-1880C>T	ENSP00000467912.2:n.291-1880C>T
ENST00000326873.12:c.367C>T MANE Select	ENSP00000324856.6:p.Gln123Ter
ENST00000652231.1:c.367C>T	ENSP00000498804.1:p.Gln123Ter
ENST00000326873.11:c.367C>T	ENSP00000324856.6:p.Gln123Ter
ENST00000585748.2:c.-6C>T	ENSP00000477641.1:n.-6C>T
ENST00000585851.1:c.291-1880C>T	ENSP00000467912.1:n.291-1880C>T
ENST00000586243.5:c.367C>T	ENSP00000467240.2:p.Gln123Ter
ENST00000586358.5:n.190C>T
ENST00000589152.5:n.457C>T
ENST00000593219.5:c.*192C>T	ENSP00000466610.1:n.*192C>T
NM_000455.4:c.367C>T , LRG_319t1:c.367C>T	NP_000446.1:p.Gln123Ter
XM_005259617.1:c.367C>T	XP_005259674.1:p.Gln123Ter
XM_005259618.3:c.367C>T	XP_005259675.1:p.Gln123Ter
XM_011528209.1:c.145C>T	XP_011526511.1:p.Gln49Ter
XR_936204.1:n.992C>T
XM_005259617.3:c.367C>T	XP_005259674.1:p.Gln123Ter
XM_011528209.2:c.145C>T	XP_011526511.1:p.Gln49Ter
XR_001753738.2:n.992C>T
XR_001753739.1:n.992C>T
XR_001753740.2:n.992C>T
NM_000455.5:c.367C>T MANE Select	NP_000446.1:p.Gln123Ter