Canonical Allele Identifier: CA402953527

Gene: STK11

Linked Data

• ClinVar Variation Id: 480720
• ClinVar RCV Id: RCV000569598 ; RCV001247509
• dbSNP Id: rs876661013
• MyVariant Identifiers: chr19:g.1226519T>G (hg19) ; chr19:g.1226520T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226520T>G , CM000681.2:g.1226520T>G	GRCh38
NC_000019.9:g.1226519T>G , CM000681.1:g.1226519T>G	GRCh37
NC_000019.8:g.1177519T>G	NCBI36
NG_007460.2:g.42114T>G , LRG_319:g.42114T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2776T>G	ENSP00000490268.2:n.*2776T>G
ENST00000585748.3:c.803T>G	ENSP00000477641.2:p.Met268Arg
ENST00000585851.2:c.1001T>G	ENSP00000467912.2:p.Met334Arg
ENST00000326873.12:c.1175T>G MANE Select	ENSP00000324856.6:p.Met392Arg
ENST00000326873.11:c.1175T>G	ENSP00000324856.6:p.Met392Arg
ENST00000585465.2:n.2908T>G
ENST00000586243.5:c.1175T>G	ENSP00000467240.2:p.Met392Arg
ENST00000589152.5:n.1873T>G
NM_000455.4:c.1175T>G , LRG_319t1:c.1175T>G	NP_000446.1:p.Met392Arg
XM_005259617.1:c.1170T>G	XP_005259674.1:p.Tyr390Ter
XM_011528209.1:c.948T>G	XP_011526511.1:p.Tyr316Ter
XM_005259617.3:c.1170T>G	XP_005259674.1:p.Tyr390Ter
XM_011528209.2:c.948T>G	XP_011526511.1:p.Tyr316Ter
XR_001753738.2:n.1981T>G
XR_001753740.2:n.1951T>G
NM_000455.5:c.1175T>G MANE Select	NP_000446.1:p.Met392Arg