Canonical Allele Identifier: CA891843673

Gene: STK11

Linked Data

• ClinVar Variation Id: 584980
• ClinVar RCV Id: RCV000709570
• dbSNP Id: rs1568689930
• MyVariant Identifiers: chr19:g.1206994dupC (hg19) ; chr19:g.1206995dupC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206995dup , CM000681.2:g.1206995dup	GRCh38
NC_000019.9:g.1206994dup , CM000681.1:g.1206994dup	GRCh37
NC_000019.8:g.1157994dup	NCBI36
NG_007460.2:g.22589dup , LRG_319:g.22589dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.82dup	ENSP00000490268.2:p.Arg28ProfsTer?
ENST00000585748.3:c.-82-11422dup	ENSP00000477641.2:n.-82-11422dup
ENST00000585851.2:c.82dup	ENSP00000467912.2:p.Arg28ProfsTer?
ENST00000326873.12:c.82dup MANE Select	ENSP00000324856.6:p.Arg28ProfsTer?
ENST00000652231.1:c.82dup	ENSP00000498804.1:p.Arg28ProfsTer?
ENST00000326873.11:c.82dup	ENSP00000324856.6:p.Arg28ProfsTer?
ENST00000585748.2:c.-82-11422dup	ENSP00000477641.1:n.-82-11422dup
ENST00000585851.1:c.82dup	ENSP00000467912.1:p.Arg28ProfsTer?
ENST00000586243.5:c.82dup	ENSP00000467240.2:p.Arg28ProfsTer?
ENST00000589152.5:n.172dup
ENST00000593219.5:c.82dup	ENSP00000466610.1:p.Arg28ProfsTer?
NM_000455.4:c.82dup , LRG_319t1:c.82dup	NP_000446.1:p.Arg28ProfsTer?
XM_005259617.1:c.82dup	XP_005259674.1:p.Arg28ProfsTer?
XM_005259618.3:c.82dup	XP_005259675.1:p.Arg28ProfsTer?
XM_011528209.1:c.-272dup	XP_011526511.1:n.-272dup
XR_936204.1:n.707dup
XM_005259617.3:c.82dup	XP_005259674.1:p.Arg28ProfsTer?
XM_011528209.2:c.-272dup	XP_011526511.1:n.-272dup
XR_001753738.2:n.707dup
XR_001753739.1:n.707dup
XR_001753740.2:n.707dup
NM_000455.5:c.82dup MANE Select	NP_000446.1:p.Arg28ProfsTer?