Canonical Allele Identifier: CA402948385

Gene: STK11

Linked Data

• ClinVar Variation Id: 484994
• ClinVar RCV Id: RCV000565289
• dbSNP Id: rs1555737824
• MyVariant Identifiers: chr19:g.1219406C>T (hg19) ; chr19:g.1219407C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219407C>T , CM000681.2:g.1219407C>T	GRCh38
NC_000019.9:g.1219406C>T , CM000681.1:g.1219406C>T	GRCh37
NC_000019.8:g.1170406C>T	NCBI36
NG_007460.2:g.35001C>T , LRG_319:g.35001C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.458C>T	ENSP00000490268.2:p.Ala153Val
ENST00000585748.3:c.86C>T	ENSP00000477641.2:p.Ala29Val
ENST00000585851.2:c.291-966C>T	ENSP00000467912.2:n.291-966C>T
ENST00000326873.12:c.458C>T MANE Select	ENSP00000324856.6:p.Ala153Val
ENST00000652231.1:c.458C>T	ENSP00000498804.1:p.Ala153Val
ENST00000326873.11:c.458C>T	ENSP00000324856.6:p.Ala153Val
ENST00000585851.1:c.291-966C>T	ENSP00000467912.1:n.291-966C>T
ENST00000586243.5:c.458C>T	ENSP00000467240.2:p.Ala153Val
ENST00000586358.5:n.281C>T
ENST00000589152.5:n.548C>T
NM_000455.4:c.458C>T , LRG_319t1:c.458C>T	NP_000446.1:p.Ala153Val
XM_005259617.1:c.458C>T	XP_005259674.1:p.Ala153Val
XM_005259618.3:c.458C>T	XP_005259675.1:p.Ala153Val
XM_011528209.1:c.236C>T	XP_011526511.1:p.Ala79Val
XR_936204.1:n.1083C>T
XM_005259617.3:c.458C>T	XP_005259674.1:p.Ala153Val
XM_011528209.2:c.236C>T	XP_011526511.1:p.Ala79Val
XR_001753738.2:n.1083C>T
XR_001753739.1:n.1083C>T
XR_001753740.2:n.1083C>T
NM_000455.5:c.458C>T MANE Select	NP_000446.1:p.Ala153Val