Canonical Allele Identifier: CA504708503

Gene: STK11

Linked Data

• dbSNP Id: rs376679847
• MyVariant Identifiers: chr19:g.1226526C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226527C>G , CM000681.2:g.1226527C>G	GRCh38
NC_000019.9:g.1226526C>G , CM000681.1:g.1226526C>G	GRCh37
NC_000019.8:g.1177526C>G	NCBI36
NG_007460.2:g.42121C>G , LRG_319:g.42121C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2783C>G	ENSP00000490268.2:n.*2783C>G
ENST00000585748.3:c.810C>G	ENSP00000477641.2:p.Gly270=
ENST00000585851.2:c.1008C>G	ENSP00000467912.2:p.Gly336=
ENST00000326873.12:c.1182C>G MANE Select	ENSP00000324856.6:p.Gly394=
ENST00000326873.11:c.1182C>G	ENSP00000324856.6:p.Gly394=
ENST00000585465.2:n.2915C>G
ENST00000586243.5:c.1182C>G	ENSP00000467240.2:p.Gly394=
ENST00000589152.5:n.1880C>G
NM_000455.4:c.1182C>G , LRG_319t1:c.1182C>G	NP_000446.1:p.Gly394=
XM_005259617.1:c.1177C>G	XP_005259674.1:p.His393Asp
XM_011528209.1:c.955C>G	XP_011526511.1:p.His319Asp
XM_005259617.3:c.1177C>G	XP_005259674.1:p.His393Asp
XM_011528209.2:c.955C>G	XP_011526511.1:p.His319Asp
XR_001753738.2:n.1988C>G
XR_001753740.2:n.1958C>G
NM_000455.5:c.1182C>G MANE Select	NP_000446.1:p.Gly394=