Canonical Allele Identifier: CA402953192

Gene: STK11

Linked Data

• ClinVar Variation Id: 2561031
• ClinVar RCV Id: RCV003300753
• dbSNP Id: rs2080821619
• MyVariant Identifiers: chr19:g.1226467G>A (hg19) ; chr19:g.1226468G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226468G>A , CM000681.2:g.1226468G>A	GRCh38
NC_000019.9:g.1226467G>A , CM000681.1:g.1226467G>A	GRCh37
NC_000019.8:g.1177467G>A	NCBI36
NG_007460.2:g.42062G>A , LRG_319:g.42062G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2724G>A	ENSP00000490268.2:n.*2724G>A
ENST00000585748.3:c.751G>A	ENSP00000477641.2:p.Glu251Lys
ENST00000585851.2:c.949G>A	ENSP00000467912.2:p.Glu317Lys
ENST00000326873.12:c.1123G>A MANE Select	ENSP00000324856.6:p.Glu375Lys
ENST00000326873.11:c.1123G>A	ENSP00000324856.6:p.Glu375Lys
ENST00000585465.2:n.2856G>A
ENST00000586243.5:c.1123G>A	ENSP00000467240.2:p.Glu375Lys
ENST00000589152.5:n.1821G>A
NM_000455.4:c.1123G>A , LRG_319t1:c.1123G>A	NP_000446.1:p.Glu375Lys
XM_005259617.1:c.1118G>A	XP_005259674.1:p.Arg373Lys
XM_011528209.1:c.896G>A	XP_011526511.1:p.Arg299Lys
XM_005259617.3:c.1118G>A	XP_005259674.1:p.Arg373Lys
XM_011528209.2:c.896G>A	XP_011526511.1:p.Arg299Lys
XR_001753738.2:n.1929G>A
XR_001753740.2:n.1899G>A
NM_000455.5:c.1123G>A MANE Select	NP_000446.1:p.Glu375Lys