Canonical Allele Identifier: CA402953893

Gene: STK11

Linked Data

• ClinVar Variation Id: 925978
• ClinVar RCV Id: RCV001188254
• dbSNP Id: rs1555740221
• MyVariant Identifiers: chr19:g.1226577C>G (hg19) ; chr19:g.1226578C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226578C>G , CM000681.2:g.1226578C>G	GRCh38
NC_000019.9:g.1226577C>G , CM000681.1:g.1226577C>G	GRCh37
NC_000019.8:g.1177577C>G	NCBI36
NG_007460.2:g.42172C>G , LRG_319:g.42172C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2834C>G	ENSP00000490268.2:n.*2834C>G
ENST00000585748.3:c.861C>G	ENSP00000477641.2:p.Pro287=
ENST00000585851.2:c.1059C>G	ENSP00000467912.2:p.Pro353=
ENST00000326873.12:c.1233C>G MANE Select	ENSP00000324856.6:p.Pro411=
ENST00000326873.11:c.1233C>G	ENSP00000324856.6:p.Pro411=
ENST00000585465.2:n.2966C>G
ENST00000586243.5:c.1232C>G	ENSP00000467240.2:p.Pro411Arg
ENST00000589152.5:n.1931C>G
NM_000455.4:c.1233C>G , LRG_319t1:c.1233C>G	NP_000446.1:p.Pro411=
XM_005259617.1:c.1228C>G	XP_005259674.1:p.Gln410Glu
XM_011528209.1:c.1006C>G	XP_011526511.1:p.Gln336Glu
XM_005259617.3:c.1228C>G	XP_005259674.1:p.Gln410Glu
XM_011528209.2:c.1006C>G	XP_011526511.1:p.Gln336Glu
XR_001753738.2:n.2039C>G
XR_001753740.2:n.2009C>G
NM_000455.5:c.1233C>G MANE Select	NP_000446.1:p.Pro411=