Canonical Allele Identifier: CA2573155835

Gene: STK11

Linked Data

• ClinVar Variation Id: 1445764
• ClinVar RCV Id: RCV001992664 ; RCV003464277
• dbSNP Id: rs2145404496

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206942dup , CM000681.2:g.1206942dup	GRCh38
NC_000019.9:g.1206941dup , CM000681.1:g.1206941dup	GRCh37
NC_000019.8:g.1157941dup	NCBI36
NG_007460.2:g.22536dup , LRG_319:g.22536dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.29dup	ENSP00000490268.2:p.Met11HisfsTer?
ENST00000585748.3:c.-82-11475dup	ENSP00000477641.2:n.-82-11475dup
ENST00000585851.2:c.29dup	ENSP00000467912.2:p.Met11HisfsTer?
ENST00000326873.12:c.29dup MANE Select	ENSP00000324856.6:p.Met11HisfsTer?
ENST00000652231.1:c.29dup	ENSP00000498804.1:p.Met11HisfsTer?
ENST00000326873.11:c.29dup	ENSP00000324856.6:p.Met11HisfsTer?
ENST00000585748.2:c.-82-11475dup	ENSP00000477641.1:n.-82-11475dup
ENST00000585851.1:c.29dup	ENSP00000467912.1:p.Met11HisfsTer?
ENST00000586243.5:c.29dup	ENSP00000467240.2:p.Met11HisfsTer?
ENST00000589152.5:n.119dup
ENST00000593219.5:c.29dup	ENSP00000466610.1:p.Met11HisfsTer?
NM_000455.4:c.29dup , LRG_319t1:c.29dup	NP_000446.1:p.Met11HisfsTer?
XM_005259617.1:c.29dup	XP_005259674.1:p.Met11HisfsTer?
XM_005259618.3:c.29dup	XP_005259675.1:p.Met11HisfsTer?
XM_011528209.1:c.-325dup	XP_011526511.1:n.-325dup
XR_936204.1:n.654dup
XM_005259617.3:c.29dup	XP_005259674.1:p.Met11HisfsTer?
XM_011528209.2:c.-325dup	XP_011526511.1:n.-325dup
XR_001753738.2:n.654dup
XR_001753739.1:n.654dup
XR_001753740.2:n.654dup
NM_000455.5:c.29dup MANE Select	NP_000446.1:p.Met11HisfsTer?