Canonical Allele Identifier: CA2537215338

Gene: STK11

Linked Data

• gnomAD v4: 19-1220826-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220831_1220832del , CM000681.2:g.1220831_1220832del	GRCh38
NC_000019.9:g.1220830_1220831del , CM000681.1:g.1220830_1220831del	GRCh37
NC_000019.8:g.1171830_1171831del	NCBI36
NG_007460.2:g.36425_36426del , LRG_319:g.36425_36426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.734+114_734+115del	ENSP00000490268.2:n.734+114_734+115del
ENST00000585748.3:c.362+114_362+115del	ENSP00000477641.2:n.362+114_362+115del
ENST00000585851.2:c.560+114_560+115del	ENSP00000467912.2:n.560+114_560+115del
ENST00000326873.12:c.734+114_734+115del MANE Select	ENSP00000324856.6:n.734+114_734+115del
ENST00000652231.1:c.734+114_734+115del	ENSP00000498804.1:n.734+114_734+115del
ENST00000326873.11:c.734+114_734+115del	ENSP00000324856.6:n.734+114_734+115del
ENST00000586243.5:c.734+114_734+115del	ENSP00000467240.2:n.734+114_734+115del
ENST00000586358.5:n.632+114_632+115del
ENST00000589152.5:n.824+114_824+115del
ENST00000591133.2:n.705+114_705+115del
NM_000455.4:c.734+114_734+115del , LRG_319t1:c.734+114_734+115del	NP_000446.1:n.734+114_734+115del
XM_005259617.1:c.734+114_734+115del	XP_005259674.1:n.734+114_734+115del
XM_005259618.3:c.734+114_734+115del	XP_005259675.1:n.734+114_734+115del
XM_011528209.1:c.512+114_512+115del	XP_011526511.1:n.512+114_512+115del
XR_936204.1:n.1359+114_1359+115del
XM_005259617.3:c.734+114_734+115del	XP_005259674.1:n.734+114_734+115del
XM_011528209.2:c.512+114_512+115del	XP_011526511.1:n.512+114_512+115del
XR_001753738.2:n.1359+114_1359+115del
XR_001753739.1:n.1359+114_1359+115del
XR_001753740.2:n.1359+114_1359+115del
NM_000455.5:c.734+114_734+115del MANE Select	NP_000446.1:n.734+114_734+115del