Canonical Allele Identifier: CA916081937

Gene: STK11

Linked Data

• ClinVar Variation Id: 848427
• ClinVar RCV Id: RCV001052181
• dbSNP Id: rs2080670808

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206997_1207010dup , CM000681.2:g.1206997_1207010dup	GRCh38
NC_000019.9:g.1206996_1207009dup , CM000681.1:g.1206996_1207009dup	GRCh37
NC_000019.8:g.1157996_1158009dup	NCBI36
NG_007460.2:g.22591_22604dup , LRG_319:g.22591_22604dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.84_97dup	ENSP00000490268.2:p.Glu33AlafsTer23
ENST00000585748.3:c.-82-11420_-82-11407dup	ENSP00000477641.2:n.-82-11420_-82-11407du...
ENST00000585851.2:c.84_97dup	ENSP00000467912.2:p.Glu33AlafsTer23
ENST00000326873.12:c.84_97dup MANE Select	ENSP00000324856.6:p.Glu33AlafsTer23
ENST00000652231.1:c.84_97dup	ENSP00000498804.1:p.Glu33AlafsTer23
ENST00000326873.11:c.84_97dup	ENSP00000324856.6:p.Glu33AlafsTer23
ENST00000585748.2:c.-82-11420_-82-11407dup	ENSP00000477641.1:n.-82-11420_-82-11407du...
ENST00000585851.1:c.84_97dup	ENSP00000467912.1:p.Glu33AlafsTer23
ENST00000586243.5:c.84_97dup	ENSP00000467240.2:p.Glu33AlafsTer23
ENST00000589152.5:n.174_187dup
ENST00000593219.5:c.84_97dup	ENSP00000466610.1:p.Glu33AlafsTer23
NM_000455.4:c.84_97dup , LRG_319t1:c.84_97dup	NP_000446.1:p.Glu33AlafsTer23
XM_005259617.1:c.84_97dup	XP_005259674.1:p.Glu33AlafsTer23
XM_005259618.3:c.84_97dup	XP_005259675.1:p.Glu33AlafsTer23
XM_011528209.1:c.-270_-257dup	XP_011526511.1:n.-270_-257dup
XR_936204.1:n.709_722dup
XM_005259617.3:c.84_97dup	XP_005259674.1:p.Glu33AlafsTer23
XM_011528209.2:c.-270_-257dup	XP_011526511.1:n.-270_-257dup
XR_001753738.2:n.709_722dup
XR_001753739.1:n.709_722dup
XR_001753740.2:n.709_722dup
NM_000455.5:c.84_97dup MANE Select	NP_000446.1:p.Glu33AlafsTer23