Canonical Allele Identifier: CA2697555600

Gene: STK11

Linked Data

• ClinVar Variation Id: 2739945
• ClinVar RCV Id: RCV003508967

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220729_1220734dup , CM000681.2:g.1220729_1220734dup	GRCh38
NC_000019.9:g.1220728_1220733dup , CM000681.1:g.1220728_1220733dup	GRCh37
NC_000019.8:g.1171728_1171733dup	NCBI36
NG_007460.2:g.36323_36328dup , LRG_319:g.36323_36328dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.734+12_734+17dup	ENSP00000490268.2:n.734+12_734+17dup
ENST00000585748.3:c.362+12_362+17dup	ENSP00000477641.2:n.362+12_362+17dup
ENST00000585851.2:c.560+12_560+17dup	ENSP00000467912.2:n.560+12_560+17dup
ENST00000326873.12:c.734+12_734+17dup MANE Select	ENSP00000324856.6:n.734+12_734+17dup
ENST00000652231.1:c.734+12_734+17dup	ENSP00000498804.1:n.734+12_734+17dup
ENST00000326873.11:c.734+12_734+17dup	ENSP00000324856.6:n.734+12_734+17dup
ENST00000586243.5:c.734+12_734+17dup	ENSP00000467240.2:n.734+12_734+17dup
ENST00000586358.5:n.632+12_632+17dup
ENST00000589152.5:n.824+12_824+17dup
ENST00000591133.2:n.705+12_705+17dup
NM_000455.4:c.734+12_734+17dup , LRG_319t1:c.734+12_734+17dup	NP_000446.1:n.734+12_734+17dup
XM_005259617.1:c.734+12_734+17dup	XP_005259674.1:n.734+12_734+17dup
XM_005259618.3:c.734+12_734+17dup	XP_005259675.1:n.734+12_734+17dup
XM_011528209.1:c.512+12_512+17dup	XP_011526511.1:n.512+12_512+17dup
XR_936204.1:n.1359+12_1359+17dup
XM_005259617.3:c.734+12_734+17dup	XP_005259674.1:n.734+12_734+17dup
XM_011528209.2:c.512+12_512+17dup	XP_011526511.1:n.512+12_512+17dup
XR_001753738.2:n.1359+12_1359+17dup
XR_001753739.1:n.1359+12_1359+17dup
XR_001753740.2:n.1359+12_1359+17dup
NM_000455.5:c.734+12_734+17dup MANE Select	NP_000446.1:n.734+12_734+17dup