Canonical Allele Identifier: CA023056

Gene: STK11

Linked Data

• ClinVar Variation Id: 7455
• ClinVar RCV Id: RCV000007881 ; RCV000434489 ; RCV002512881
• dbSNP Id: rs121913323
• COSMIC: COSM20943
• MyVariant Identifiers: chr19:g.1220415C>T (hg19) ; chr19:g.1220416C>T (hg38)
• PubMed: PMID:10208439 ; PMID:25157968

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220416C>T , CM000681.2:g.1220416C>T	GRCh38
NC_000019.9:g.1220415C>T , CM000681.1:g.1220415C>T	GRCh37
NC_000019.8:g.1171415C>T	NCBI36
NG_007460.2:g.36010C>T , LRG_319:g.36010C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.508C>T	ENSP00000490268.2:p.Gln170Ter
ENST00000585748.3:c.136C>T	ENSP00000477641.2:p.Gln46Ter
ENST00000585851.2:c.334C>T	ENSP00000467912.2:p.Gln112Ter
ENST00000326873.12:c.508C>T MANE Select	ENSP00000324856.6:p.Gln170Ter
ENST00000652231.1:c.508C>T	ENSP00000498804.1:p.Gln170Ter
ENST00000326873.11:c.508C>T	ENSP00000324856.6:p.Gln170Ter
ENST00000585851.1:c.334C>T	ENSP00000467912.1:p.Gln112Ter
ENST00000586243.5:c.508C>T	ENSP00000467240.2:p.Gln170Ter
ENST00000586358.5:n.331C>T
ENST00000589152.5:n.598C>T
ENST00000591133.2:n.404C>T
NM_000455.4:c.508C>T , LRG_319t1:c.508C>T	NP_000446.1:p.Gln170Ter
XM_005259617.1:c.508C>T	XP_005259674.1:p.Gln170Ter
XM_005259618.3:c.508C>T	XP_005259675.1:p.Gln170Ter
XM_011528209.1:c.286C>T	XP_011526511.1:p.Gln96Ter
XR_936204.1:n.1133C>T
XM_005259617.3:c.508C>T	XP_005259674.1:p.Gln170Ter
XM_011528209.2:c.286C>T	XP_011526511.1:p.Gln96Ter
XR_001753738.2:n.1133C>T
XR_001753739.1:n.1133C>T
XR_001753740.2:n.1133C>T
NM_000455.5:c.508C>T MANE Select	NP_000446.1:p.Gln170Ter