Canonical Allele Identifier: CA10586687

Gene: STK11

Linked Data

• ClinVar Variation Id: 254654
• ClinVar RCV Id: RCV000241351 ; RCV000492112
• dbSNP Id: rs886037859
• MyVariant Identifiers: chr19:g.1220449A>G (hg19) ; chr19:g.1220450A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220450A>G , CM000681.2:g.1220450A>G	GRCh38
NC_000019.9:g.1220449A>G , CM000681.1:g.1220449A>G	GRCh37
NC_000019.8:g.1171449A>G	NCBI36
NG_007460.2:g.36044A>G , LRG_319:g.36044A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.542A>G	ENSP00000490268.2:p.Asn181Ser
ENST00000585748.3:c.170A>G	ENSP00000477641.2:p.Asn57Ser
ENST00000585851.2:c.368A>G	ENSP00000467912.2:p.Asn123Ser
ENST00000326873.12:c.542A>G MANE Select	ENSP00000324856.6:p.Asn181Ser
ENST00000652231.1:c.542A>G	ENSP00000498804.1:p.Asn181Ser
ENST00000326873.11:c.542A>G	ENSP00000324856.6:p.Asn181Ser
ENST00000585851.1:c.368A>G	ENSP00000467912.1:p.Asn123Ser
ENST00000586243.5:c.542A>G	ENSP00000467240.2:p.Asn181Ser
ENST00000586358.5:n.365A>G
ENST00000589152.5:n.632A>G
ENST00000591133.2:n.438A>G
NM_000455.4:c.542A>G , LRG_319t1:c.542A>G	NP_000446.1:p.Asn181Ser
XM_005259617.1:c.542A>G	XP_005259674.1:p.Asn181Ser
XM_005259618.3:c.542A>G	XP_005259675.1:p.Asn181Ser
XM_011528209.1:c.320A>G	XP_011526511.1:p.Asn107Ser
XR_936204.1:n.1167A>G
XM_005259617.3:c.542A>G	XP_005259674.1:p.Asn181Ser
XM_011528209.2:c.320A>G	XP_011526511.1:p.Asn107Ser
XR_001753738.2:n.1167A>G
XR_001753739.1:n.1167A>G
XR_001753740.2:n.1167A>G
NM_000455.5:c.542A>G MANE Select	NP_000446.1:p.Asn181Ser