Canonical Allele Identifier: CA2582592836

Gene: STK11

Linked Data

• gnomAD v4: 19-1220309-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220312del , CM000681.2:g.1220312del	GRCh38
NC_000019.9:g.1220311del , CM000681.1:g.1220311del	GRCh37
NC_000019.8:g.1171311del	NCBI36
NG_007460.2:g.35906del , LRG_319:g.35906del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.465-61del	ENSP00000490268.2:n.465-61del
ENST00000585748.3:c.93-61del	ENSP00000477641.2:n.93-61del
ENST00000585851.2:c.291-61del	ENSP00000467912.2:n.291-61del
ENST00000326873.12:c.465-61del MANE Select	ENSP00000324856.6:n.465-61del
ENST00000652231.1:c.465-61del	ENSP00000498804.1:n.465-61del
ENST00000326873.11:c.465-61del	ENSP00000324856.6:n.465-61del
ENST00000585851.1:c.291-61del	ENSP00000467912.1:n.291-61del
ENST00000586243.5:c.465-61del	ENSP00000467240.2:n.465-61del
ENST00000586358.5:n.288-61del
ENST00000589152.5:n.555-61del
ENST00000591133.2:n.300del
NM_000455.4:c.465-61del , LRG_319t1:c.465-61del	NP_000446.1:n.465-61del
XM_005259617.1:c.465-61del	XP_005259674.1:n.465-61del
XM_005259618.3:c.465-61del	XP_005259675.1:n.465-61del
XM_011528209.1:c.243-61del	XP_011526511.1:n.243-61del
XR_936204.1:n.1090-61del
XM_005259617.3:c.465-61del	XP_005259674.1:n.465-61del
XM_011528209.2:c.243-61del	XP_011526511.1:n.243-61del
XR_001753738.2:n.1090-61del
XR_001753739.1:n.1090-61del
XR_001753740.2:n.1090-61del
NM_000455.5:c.465-61del MANE Select	NP_000446.1:n.465-61del