Canonical Allele Identifier: CA402954128

Gene: STK11

Linked Data

• ClinVar Variation Id: 492516
• ClinVar RCV Id: RCV000582770 ; RCV001860103
• dbSNP Id: rs1555740268
• MyVariant Identifiers: chr19:g.1226611A>G (hg19) ; chr19:g.1226612A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226612A>G , CM000681.2:g.1226612A>G	GRCh38
NC_000019.9:g.1226611A>G , CM000681.1:g.1226611A>G	GRCh37
NC_000019.8:g.1177611A>G	NCBI36
NG_007460.2:g.42206A>G , LRG_319:g.42206A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2868A>G	ENSP00000490268.2:n.*2868A>G
ENST00000585748.3:c.895A>G	ENSP00000477641.2:p.Lys299Glu
ENST00000585851.2:c.1093A>G	ENSP00000467912.2:p.Lys365Glu
ENST00000326873.12:c.1267A>G MANE Select	ENSP00000324856.6:p.Lys423Glu
ENST00000326873.11:c.1267A>G	ENSP00000324856.6:p.Lys423Glu
ENST00000585465.2:n.3000A>G
ENST00000586243.5:c.1264A>G	ENSP00000467240.2:p.Lys422Glu
ENST00000589152.5:n.1965A>G
NM_000455.4:c.1267A>G , LRG_319t1:c.1267A>G	NP_000446.1:p.Lys423Glu
XM_005259617.1:c.1262A>G	XP_005259674.1:p.Gln421Arg
XM_011528209.1:c.1040A>G	XP_011526511.1:p.Gln347Arg
XM_005259617.3:c.1262A>G	XP_005259674.1:p.Gln421Arg
XM_011528209.2:c.1040A>G	XP_011526511.1:p.Gln347Arg
XR_001753738.2:n.2073A>G
XR_001753740.2:n.2043A>G
NM_000455.5:c.1267A>G MANE Select	NP_000446.1:p.Lys423Glu