Canonical Allele Identifier: CA913188991

Gene: STK11

Linked Data

• ClinVar Variation Id: 628221
• ClinVar RCV Id: RCV000772564
• dbSNP Id: rs1599929369

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223046_1223047del , CM000681.2:g.1223046_1223047del	GRCh38
NC_000019.9:g.1223045_1223046del , CM000681.1:g.1223045_1223046del	GRCh37
NC_000019.8:g.1174045_1174046del	NCBI36
NG_007460.2:g.38640_38641del , LRG_319:g.38640_38641del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.982_983del	ENSP00000490268.2:p.Thr328GlnfsTer?
ENST00000585748.3:c.610_611del	ENSP00000477641.2:p.Thr204GlnfsTer?
ENST00000585851.2:c.808_809del	ENSP00000467912.2:p.Thr270GlnfsTer?
ENST00000326873.12:c.982_983del MANE Select	ENSP00000324856.6:p.Thr328GlnfsTer?
ENST00000652231.1:c.982_983del	ENSP00000498804.1:p.Thr328GlnfsTer?
ENST00000326873.11:c.982_983del	ENSP00000324856.6:p.Thr328GlnfsTer?
ENST00000586243.5:c.982_983del	ENSP00000467240.2:p.Thr328GlnfsTer?
ENST00000589152.5:n.1680_1681del
ENST00000591133.2:n.953_954del
NM_000455.4:c.982_983del , LRG_319t1:c.982_983del	NP_000446.1:p.Thr328GlnfsTer?
XM_005259617.1:c.982_983del	XP_005259674.1:p.Thr328GlnfsTer?
XM_005259618.3:c.982_983del	XP_005259675.1:p.Thr328GlnfsTer?
XM_011528209.1:c.760_761del	XP_011526511.1:p.Thr254GlnfsTer?
XR_936204.1:n.1758_1759del
XM_005259617.3:c.982_983del	XP_005259674.1:p.Thr328GlnfsTer?
XM_011528209.2:c.760_761del	XP_011526511.1:p.Thr254GlnfsTer?
XR_001753738.2:n.1788_1789del
XR_001753739.1:n.1788_1789del
XR_001753740.2:n.1758_1759del
NM_000455.5:c.982_983del MANE Select	NP_000446.1:p.Thr328GlnfsTer?