Canonical Allele Identifier: CA504707259

Gene: STK11

Linked Data

• ClinVar Variation Id: 1762723
• ClinVar RCV Id: RCV002412566
• COSMIC: COSM25850
• MyVariant Identifiers: chr19:g.1221304del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221305del , CM000681.2:g.1221305del	GRCh38
NC_000019.9:g.1221304del , CM000681.1:g.1221304del	GRCh37
NC_000019.8:g.1172304del	NCBI36
NG_007460.2:g.36899del , LRG_319:g.36899del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.827del	ENSP00000490268.2:p.Gly276AlafsTer11
ENST00000585748.3:c.455del	ENSP00000477641.2:p.Gly152AlafsTer11
ENST00000585851.2:c.653del	ENSP00000467912.2:p.Gly218AlafsTer11
ENST00000326873.12:c.827del MANE Select	ENSP00000324856.6:p.Gly276AlafsTer11
ENST00000652231.1:c.827del	ENSP00000498804.1:p.Gly276AlafsTer11
ENST00000326873.11:c.827del	ENSP00000324856.6:p.Gly276AlafsTer11
ENST00000586243.5:c.827del	ENSP00000467240.2:p.Gly276AlafsTer11
ENST00000586358.5:n.725del
ENST00000589152.5:n.917del
ENST00000591133.2:n.798del
NM_000455.4:c.827del , LRG_319t1:c.827del	NP_000446.1:p.Gly276AlafsTer11
XM_005259617.1:c.827del	XP_005259674.1:p.Gly276AlafsTer11
XM_005259618.3:c.827del	XP_005259675.1:p.Gly276AlafsTer11
XM_011528209.1:c.605del	XP_011526511.1:p.Gly202AlafsTer11
XR_936204.1:n.1452del
XM_005259617.3:c.827del	XP_005259674.1:p.Gly276AlafsTer11
XM_011528209.2:c.605del	XP_011526511.1:p.Gly202AlafsTer11
XR_001753738.2:n.1452del
XR_001753739.1:n.1452del
XR_001753740.2:n.1452del
NM_000455.5:c.827del MANE Select	NP_000446.1:p.Gly276AlafsTer11