Canonical Allele Identifier: CA2582597021

Gene: STK11

Linked Data

• gnomAD v4: 19-1226226-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226230del , CM000681.2:g.1226230del	GRCh38
NC_000019.9:g.1226229del , CM000681.1:g.1226229del	GRCh37
NC_000019.8:g.1177229del	NCBI36
NG_007460.2:g.41824del , LRG_319:g.41824del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2486del	ENSP00000490268.2:n.*2486del
ENST00000585748.3:c.737-224del	ENSP00000477641.2:n.737-224del
ENST00000585851.2:c.935-224del	ENSP00000467912.2:n.935-224del
ENST00000326873.12:c.1109-224del MANE Select	ENSP00000324856.6:n.1109-224del
ENST00000326873.11:c.1109-224del	ENSP00000324856.6:n.1109-224del
ENST00000585465.2:n.2618del
ENST00000586243.5:c.1109-224del	ENSP00000467240.2:n.1109-224del
ENST00000589152.5:n.1807-224del
NM_000455.4:c.1109-224del , LRG_319t1:c.1109-224del	NP_000446.1:n.1109-224del
XM_005259617.1:c.1109-229del	XP_005259674.1:n.1109-229del
XM_011528209.1:c.887-229del	XP_011526511.1:n.887-229del
XM_005259617.3:c.1109-229del	XP_005259674.1:n.1109-229del
XM_011528209.2:c.887-229del	XP_011526511.1:n.887-229del
XR_001753738.2:n.1915-224del
XR_001753740.2:n.1885-224del
NM_000455.5:c.1109-224del MANE Select	NP_000446.1:n.1109-224del