Canonical Allele Identifier: CA402949748

Gene: STK11

Linked Data

• ClinVar Variation Id: 843985
• ClinVar RCV Id: RCV001046718
• dbSNP Id: rs748832988
• MyVariant Identifiers: chr19:g.1220660C>A (hg19) ; chr19:g.1220661C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220661C>A , CM000681.2:g.1220661C>A	GRCh38
NC_000019.9:g.1220660C>A , CM000681.1:g.1220660C>A	GRCh37
NC_000019.8:g.1171660C>A	NCBI36
NG_007460.2:g.36255C>A , LRG_319:g.36255C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.678C>A	ENSP00000490268.2:p.Asn226Lys
ENST00000585748.3:c.306C>A	ENSP00000477641.2:p.Asn102Lys
ENST00000585851.2:c.504C>A	ENSP00000467912.2:p.Asn168Lys
ENST00000326873.12:c.678C>A MANE Select	ENSP00000324856.6:p.Asn226Lys
ENST00000652231.1:c.678C>A	ENSP00000498804.1:p.Asn226Lys
ENST00000326873.11:c.678C>A	ENSP00000324856.6:p.Asn226Lys
ENST00000586243.5:c.678C>A	ENSP00000467240.2:p.Asn226Lys
ENST00000586358.5:n.576C>A
ENST00000589152.5:n.768C>A
ENST00000591133.2:n.649C>A
NM_000455.4:c.678C>A , LRG_319t1:c.678C>A	NP_000446.1:p.Asn226Lys
XM_005259617.1:c.678C>A	XP_005259674.1:p.Asn226Lys
XM_005259618.3:c.678C>A	XP_005259675.1:p.Asn226Lys
XM_011528209.1:c.456C>A	XP_011526511.1:p.Asn152Lys
XR_936204.1:n.1303C>A
XM_005259617.3:c.678C>A	XP_005259674.1:p.Asn226Lys
XM_011528209.2:c.456C>A	XP_011526511.1:p.Asn152Lys
XR_001753738.2:n.1303C>A
XR_001753739.1:n.1303C>A
XR_001753740.2:n.1303C>A
NM_000455.5:c.678C>A MANE Select	NP_000446.1:p.Asn226Lys