Canonical Allele Identifier: CA2573155760

Gene: STK11

Linked Data

• ClinVar Variation Id: 1456978
• ClinVar RCV Id: RCV001972514
• dbSNP Id: rs2145424194

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220395_1220398dup , CM000681.2:g.1220395_1220398dup	GRCh38
NC_000019.9:g.1220394_1220397dup , CM000681.1:g.1220394_1220397dup	GRCh37
NC_000019.8:g.1171394_1171397dup	NCBI36
NG_007460.2:g.35989_35992dup , LRG_319:g.35989_35992dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.487_490dup	ENSP00000490268.2:p.Leu164ArgfsTer7
ENST00000585748.3:c.115_118dup	ENSP00000477641.2:p.Leu40ArgfsTer7
ENST00000585851.2:c.313_316dup	ENSP00000467912.2:p.Leu106ArgfsTer7
ENST00000326873.12:c.487_490dup MANE Select	ENSP00000324856.6:p.Leu164ArgfsTer7
ENST00000652231.1:c.487_490dup	ENSP00000498804.1:p.Leu164ArgfsTer7
ENST00000326873.11:c.487_490dup	ENSP00000324856.6:p.Leu164ArgfsTer7
ENST00000585851.1:c.313_316dup	ENSP00000467912.1:p.Leu106ArgfsTer7
ENST00000586243.5:c.487_490dup	ENSP00000467240.2:p.Leu164ArgfsTer7
ENST00000586358.5:n.310_313dup
ENST00000589152.5:n.577_580dup
ENST00000591133.2:n.383_386dup
NM_000455.4:c.487_490dup , LRG_319t1:c.487_490dup	NP_000446.1:p.Leu164ArgfsTer7
XM_005259617.1:c.487_490dup	XP_005259674.1:p.Leu164ArgfsTer7
XM_005259618.3:c.487_490dup	XP_005259675.1:p.Leu164ArgfsTer7
XM_011528209.1:c.265_268dup	XP_011526511.1:p.Leu90ArgfsTer7
XR_936204.1:n.1112_1115dup
XM_005259617.3:c.487_490dup	XP_005259674.1:p.Leu164ArgfsTer7
XM_011528209.2:c.265_268dup	XP_011526511.1:p.Leu90ArgfsTer7
XR_001753738.2:n.1112_1115dup
XR_001753739.1:n.1112_1115dup
XR_001753740.2:n.1112_1115dup
NM_000455.5:c.487_490dup MANE Select	NP_000446.1:p.Leu164ArgfsTer7