Canonical Allele Identifier: CA504707328

Gene: STK11

Linked Data

• ClinVar Variation Id: 2586609
• ClinVar RCV Id: RCV003358374
• MyVariant Identifiers: chr19:g.1221326T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221327T>G , CM000681.2:g.1221327T>G	GRCh38
NC_000019.9:g.1221326T>G , CM000681.1:g.1221326T>G	GRCh37
NC_000019.8:g.1172326T>G	NCBI36
NG_007460.2:g.36921T>G , LRG_319:g.36921T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.849T>G	ENSP00000490268.2:p.Ser283=
ENST00000585748.3:c.477T>G	ENSP00000477641.2:p.Ser159=
ENST00000585851.2:c.675T>G	ENSP00000467912.2:p.Ser225=
ENST00000326873.12:c.849T>G MANE Select	ENSP00000324856.6:p.Ser283=
ENST00000652231.1:c.849T>G	ENSP00000498804.1:p.Ser283=
ENST00000326873.11:c.849T>G	ENSP00000324856.6:p.Ser283=
ENST00000586243.5:c.849T>G	ENSP00000467240.2:p.Ser283=
ENST00000586358.5:n.747T>G
ENST00000589152.5:n.939T>G
ENST00000591133.2:n.820T>G
NM_000455.4:c.849T>G , LRG_319t1:c.849T>G	NP_000446.1:p.Ser283=
XM_005259617.1:c.849T>G	XP_005259674.1:p.Ser283=
XM_005259618.3:c.849T>G	XP_005259675.1:p.Ser283=
XM_011528209.1:c.627T>G	XP_011526511.1:p.Ser209=
XR_936204.1:n.1474T>G
XM_005259617.3:c.849T>G	XP_005259674.1:p.Ser283=
XM_011528209.2:c.627T>G	XP_011526511.1:p.Ser209=
XR_001753738.2:n.1474T>G
XR_001753739.1:n.1474T>G
XR_001753740.2:n.1474T>G
NM_000455.5:c.849T>G MANE Select	NP_000446.1:p.Ser283=