Canonical Allele Identifier: CA2697555611

Gene: STK11

Linked Data

• ClinVar Variation Id: 2745061
• ClinVar RCV Id: RCV003506866

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226539dup , CM000681.2:g.1226539dup	GRCh38
NC_000019.9:g.1226538dup , CM000681.1:g.1226538dup	GRCh37
NC_000019.8:g.1177538dup	NCBI36
NG_007460.2:g.42133dup , LRG_319:g.42133dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2795dup	ENSP00000490268.2:n.*2795dup
ENST00000585748.3:c.822dup	ENSP00000477641.2:p.Gln275AlafsTer?
ENST00000585851.2:c.1020dup	ENSP00000467912.2:p.Gln341AlafsTer?
ENST00000326873.12:c.1194dup MANE Select	ENSP00000324856.6:p.Gln399AlafsTer?
ENST00000326873.11:c.1194dup	ENSP00000324856.6:p.Gln399AlafsTer?
ENST00000585465.2:n.2927dup
ENST00000586243.5:c.1194dup	ENSP00000467240.2:p.Gln399AlafsTer?
ENST00000589152.5:n.1892dup
NM_000455.4:c.1194dup , LRG_319t1:c.1194dup	NP_000446.1:p.Gln399AlafsTer?
XM_005259617.1:c.1189dup	XP_005259674.1:p.Ala397GlyfsTer3
XM_011528209.1:c.967dup	XP_011526511.1:p.Ala323GlyfsTer3
XM_005259617.3:c.1189dup	XP_005259674.1:p.Ala397GlyfsTer3
XM_011528209.2:c.967dup	XP_011526511.1:p.Ala323GlyfsTer3
XR_001753738.2:n.2000dup
XR_001753740.2:n.1970dup
NM_000455.5:c.1194dup MANE Select	NP_000446.1:p.Gln399AlafsTer?