Canonical Allele Identifier: CA402949993

Gene: STK11

Linked Data

• ClinVar Variation Id: 458059
• ClinVar RCV Id: RCV000550258
• dbSNP Id: rs1555738476
• MyVariant Identifiers: chr19:g.1220713C>A (hg19) ; chr19:g.1220714C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220714C>A , CM000681.2:g.1220714C>A	GRCh38
NC_000019.9:g.1220713C>A , CM000681.1:g.1220713C>A	GRCh37
NC_000019.8:g.1171713C>A	NCBI36
NG_007460.2:g.36308C>A , LRG_319:g.36308C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.731C>A	ENSP00000490268.2:p.Thr244Asn
ENST00000585748.3:c.359C>A	ENSP00000477641.2:p.Thr120Asn
ENST00000585851.2:c.557C>A	ENSP00000467912.2:p.Thr186Asn
ENST00000326873.12:c.731C>A MANE Select	ENSP00000324856.6:p.Thr244Asn
ENST00000652231.1:c.731C>A	ENSP00000498804.1:p.Thr244Asn
ENST00000326873.11:c.731C>A	ENSP00000324856.6:p.Thr244Asn
ENST00000586243.5:c.731C>A	ENSP00000467240.2:p.Thr244Asn
ENST00000586358.5:n.629C>A
ENST00000589152.5:n.821C>A
ENST00000591133.2:n.702C>A
NM_000455.4:c.731C>A , LRG_319t1:c.731C>A	NP_000446.1:p.Thr244Asn
XM_005259617.1:c.731C>A	XP_005259674.1:p.Thr244Asn
XM_005259618.3:c.731C>A	XP_005259675.1:p.Thr244Asn
XM_011528209.1:c.509C>A	XP_011526511.1:p.Thr170Asn
XR_936204.1:n.1356C>A
XM_005259617.3:c.731C>A	XP_005259674.1:p.Thr244Asn
XM_011528209.2:c.509C>A	XP_011526511.1:p.Thr170Asn
XR_001753738.2:n.1356C>A
XR_001753739.1:n.1356C>A
XR_001753740.2:n.1356C>A
NM_000455.5:c.731C>A MANE Select	NP_000446.1:p.Thr244Asn