Canonical Allele Identifier: CA504708549

Gene: STK11

Linked Data

• ClinVar Variation Id: 1541473
• ClinVar RCV Id: RCV002157436
• dbSNP Id: rs2145436544
• gnomAD v4: 19-1226617-C-A
• MyVariant Identifiers: chr19:g.1226616C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226617C>A , CM000681.2:g.1226617C>A	GRCh38
NC_000019.9:g.1226616C>A , CM000681.1:g.1226616C>A	GRCh37
NC_000019.8:g.1177616C>A	NCBI36
NG_007460.2:g.42211C>A , LRG_319:g.42211C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2873C>A	ENSP00000490268.2:n.*2873C>A
ENST00000585748.3:c.900C>A	ENSP00000477641.2:p.Ile300=
ENST00000585851.2:c.1098C>A	ENSP00000467912.2:p.Ile366=
ENST00000326873.12:c.1272C>A MANE Select	ENSP00000324856.6:p.Ile424=
ENST00000326873.11:c.1272C>A	ENSP00000324856.6:p.Ile424=
ENST00000585465.2:n.3005C>A
ENST00000586243.5:c.1269C>A	ENSP00000467240.2:p.Ile423=
ENST00000589152.5:n.1970C>A
NM_000455.4:c.1272C>A , LRG_319t1:c.1272C>A	NP_000446.1:p.Ile424=
XM_005259617.1:c.1267C>A	XP_005259674.1:p.Pro423Thr
XM_011528209.1:c.1045C>A	XP_011526511.1:p.Pro349Thr
XM_005259617.3:c.1267C>A	XP_005259674.1:p.Pro423Thr
XM_011528209.2:c.1045C>A	XP_011526511.1:p.Pro349Thr
XR_001753738.2:n.2078C>A
XR_001753740.2:n.2048C>A
NM_000455.5:c.1272C>A MANE Select	NP_000446.1:p.Ile424=