Canonical Allele Identifier: CA2582592890

Gene: STK11

Linked Data

• gnomAD v4: 19-1220344-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220348del , CM000681.2:g.1220348del	GRCh38
NC_000019.9:g.1220347del , CM000681.1:g.1220347del	GRCh37
NC_000019.8:g.1171347del	NCBI36
NG_007460.2:g.35942del , LRG_319:g.35942del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.465-25del	ENSP00000490268.2:n.465-25del
ENST00000585748.3:c.93-25del	ENSP00000477641.2:n.93-25del
ENST00000585851.2:c.291-25del	ENSP00000467912.2:n.291-25del
ENST00000326873.12:c.465-25del MANE Select	ENSP00000324856.6:n.465-25del
ENST00000652231.1:c.465-25del	ENSP00000498804.1:n.465-25del
ENST00000326873.11:c.465-25del	ENSP00000324856.6:n.465-25del
ENST00000585851.1:c.291-25del	ENSP00000467912.1:n.291-25del
ENST00000586243.5:c.465-25del	ENSP00000467240.2:n.465-25del
ENST00000586358.5:n.288-25del
ENST00000589152.5:n.555-25del
ENST00000591133.2:n.336del
NM_000455.4:c.465-25del , LRG_319t1:c.465-25del	NP_000446.1:n.465-25del
XM_005259617.1:c.465-25del	XP_005259674.1:n.465-25del
XM_005259618.3:c.465-25del	XP_005259675.1:n.465-25del
XM_011528209.1:c.243-25del	XP_011526511.1:n.243-25del
XR_936204.1:n.1090-25del
XM_005259617.3:c.465-25del	XP_005259674.1:n.465-25del
XM_011528209.2:c.243-25del	XP_011526511.1:n.243-25del
XR_001753738.2:n.1090-25del
XR_001753739.1:n.1090-25del
XR_001753740.2:n.1090-25del
NM_000455.5:c.465-25del MANE Select	NP_000446.1:n.465-25del