Canonical Allele Identifier: CA402953408

Gene: STK11

Linked Data

• ClinVar Variation Id: 1365767
• ClinVar RCV Id: RCV001942770
• dbSNP Id: rs2145435992
• MyVariant Identifiers: chr19:g.1226500C>A (hg19) ; chr19:g.1226501C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226501C>A , CM000681.2:g.1226501C>A	GRCh38
NC_000019.9:g.1226500C>A , CM000681.1:g.1226500C>A	GRCh37
NC_000019.8:g.1177500C>A	NCBI36
NG_007460.2:g.42095C>A , LRG_319:g.42095C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2757C>A	ENSP00000490268.2:n.*2757C>A
ENST00000585748.3:c.784C>A	ENSP00000477641.2:p.Leu262Ile
ENST00000585851.2:c.982C>A	ENSP00000467912.2:p.Leu328Ile
ENST00000326873.12:c.1156C>A MANE Select	ENSP00000324856.6:p.Leu386Ile
ENST00000326873.11:c.1156C>A	ENSP00000324856.6:p.Leu386Ile
ENST00000585465.2:n.2889C>A
ENST00000586243.5:c.1156C>A	ENSP00000467240.2:p.Leu386Ile
ENST00000589152.5:n.1854C>A
NM_000455.4:c.1156C>A , LRG_319t1:c.1156C>A	NP_000446.1:p.Leu386Ile
XM_005259617.1:c.1151C>A	XP_005259674.1:p.Pro384His
XM_011528209.1:c.929C>A	XP_011526511.1:p.Pro310His
XM_005259617.3:c.1151C>A	XP_005259674.1:p.Pro384His
XM_011528209.2:c.929C>A	XP_011526511.1:p.Pro310His
XR_001753738.2:n.1962C>A
XR_001753740.2:n.1932C>A
NM_000455.5:c.1156C>A MANE Select	NP_000446.1:p.Leu386Ile