Canonical Allele Identifier: CA2966063660

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226598dup , CM000681.2:g.1226598dup	GRCh38
NC_000019.9:g.1226597dup , CM000681.1:g.1226597dup	GRCh37
NC_000019.8:g.1177597dup	NCBI36
NG_007460.2:g.42192dup , LRG_319:g.42192dup

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1253dup MANE Select	NP_000446.1:p.Cys418TrpfsTer?
ENST00000326873.12:c.1253dup MANE Select	ENSP00000324856.6:p.Cys418TrpfsTer?
NM_000455.4:c.1253dup , LRG_319t1:c.1253dup	NP_000446.1:p.Cys418TrpfsTer?
ENST00000326873.11:c.1253dup	ENSP00000324856.6:p.Cys418TrpfsTer?
ENST00000585465.2:n.2986dup
ENST00000585465.3:c.*2854dup	ENSP00000490268.2:n.*2854dup
ENST00000585748.3:c.881dup	ENSP00000477641.2:p.Cys294TrpfsTer?
ENST00000585851.2:c.1079dup	ENSP00000467912.2:p.Cys360TrpfsTer?
ENST00000586243.5:c.1252dup	ENSP00000467240.2:p.Ala418GlyfsTer?
ENST00000589152.5:n.1951dup
XM_005259617.1:c.1248dup	XP_005259674.1:p.Leu417AlafsTer?
XM_005259617.3:c.1248dup	XP_005259674.1:p.Leu417AlafsTer?
XM_011528209.1:c.1026dup	XP_011526511.1:p.Leu343AlafsTer?
XM_011528209.2:c.1026dup	XP_011526511.1:p.Leu343AlafsTer?
XR_001753738.2:n.2059dup
XR_001753740.2:n.2029dup