Canonical Allele Identifier: CA2582593058

Gene: STK11

Linked Data

• gnomAD v4: 19-1220838-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220839del , CM000681.2:g.1220839del	GRCh38
NC_000019.9:g.1220838del , CM000681.1:g.1220838del	GRCh37
NC_000019.8:g.1171838del	NCBI36
NG_007460.2:g.36433del , LRG_319:g.36433del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.734+122del	ENSP00000490268.2:n.734+122del
ENST00000585748.3:c.362+122del	ENSP00000477641.2:n.362+122del
ENST00000585851.2:c.560+122del	ENSP00000467912.2:n.560+122del
ENST00000326873.12:c.734+122del MANE Select	ENSP00000324856.6:n.734+122del
ENST00000652231.1:c.734+122del	ENSP00000498804.1:n.734+122del
ENST00000326873.11:c.734+122del	ENSP00000324856.6:n.734+122del
ENST00000586243.5:c.734+122del	ENSP00000467240.2:n.734+122del
ENST00000586358.5:n.632+122del
ENST00000589152.5:n.824+122del
ENST00000591133.2:n.705+122del
NM_000455.4:c.734+122del , LRG_319t1:c.734+122del	NP_000446.1:n.734+122del
XM_005259617.1:c.734+122del	XP_005259674.1:n.734+122del
XM_005259618.3:c.734+122del	XP_005259675.1:n.734+122del
XM_011528209.1:c.512+122del	XP_011526511.1:n.512+122del
XR_936204.1:n.1359+122del
XM_005259617.3:c.734+122del	XP_005259674.1:n.734+122del
XM_011528209.2:c.512+122del	XP_011526511.1:n.512+122del
XR_001753738.2:n.1359+122del
XR_001753739.1:n.1359+122del
XR_001753740.2:n.1359+122del
NM_000455.5:c.734+122del MANE Select	NP_000446.1:n.734+122del