Canonical Allele Identifier: CA2576546361

Gene: STK11

Linked Data

• gnomAD v4: 19-1220811-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220813del , CM000681.2:g.1220813del	GRCh38
NC_000019.9:g.1220812del , CM000681.1:g.1220812del	GRCh37
NC_000019.8:g.1171812del	NCBI36
NG_007460.2:g.36407del , LRG_319:g.36407del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.734+96del	ENSP00000490268.2:n.734+96del
ENST00000585748.3:c.362+96del	ENSP00000477641.2:n.362+96del
ENST00000585851.2:c.560+96del	ENSP00000467912.2:n.560+96del
ENST00000326873.12:c.734+96del MANE Select	ENSP00000324856.6:n.734+96del
ENST00000652231.1:c.734+96del	ENSP00000498804.1:n.734+96del
ENST00000326873.11:c.734+96del	ENSP00000324856.6:n.734+96del
ENST00000586243.5:c.734+96del	ENSP00000467240.2:n.734+96del
ENST00000586358.5:n.632+96del
ENST00000589152.5:n.824+96del
ENST00000591133.2:n.705+96del
NM_000455.4:c.734+96del , LRG_319t1:c.734+96del	NP_000446.1:n.734+96del
XM_005259617.1:c.734+96del	XP_005259674.1:n.734+96del
XM_005259618.3:c.734+96del	XP_005259675.1:n.734+96del
XM_011528209.1:c.512+96del	XP_011526511.1:n.512+96del
XR_936204.1:n.1359+96del
XM_005259617.3:c.734+96del	XP_005259674.1:n.734+96del
XM_011528209.2:c.512+96del	XP_011526511.1:n.512+96del
XR_001753738.2:n.1359+96del
XR_001753739.1:n.1359+96del
XR_001753740.2:n.1359+96del
NM_000455.5:c.734+96del MANE Select	NP_000446.1:n.734+96del