Canonical Allele Identifier: CA783335177

Gene: STK11

Linked Data

• dbSNP Id: rs1159506952
• gnomAD v3: 19-1220745-AC-A
• gnomAD v4: 19-1220745-AC-A
• MyVariant Identifiers: chr19:g.1220745del (hg19) ; chr19:g.1220746del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220747del , CM000681.2:g.1220747del	GRCh38
NC_000019.9:g.1220746del , CM000681.1:g.1220746del	GRCh37
NC_000019.8:g.1171746del	NCBI36
NG_007460.2:g.36341del , LRG_319:g.36341del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.734+30del	ENSP00000490268.2:n.734+30del
ENST00000585748.3:c.362+30del	ENSP00000477641.2:n.362+30del
ENST00000585851.2:c.560+30del	ENSP00000467912.2:n.560+30del
ENST00000326873.12:c.734+30del MANE Select	ENSP00000324856.6:n.734+30del
ENST00000652231.1:c.734+30del	ENSP00000498804.1:n.734+30del
ENST00000326873.11:c.734+30del	ENSP00000324856.6:n.734+30del
ENST00000586243.5:c.734+30del	ENSP00000467240.2:n.734+30del
ENST00000586358.5:n.632+30del
ENST00000589152.5:n.824+30del
ENST00000591133.2:n.705+30del
NM_000455.4:c.734+30del , LRG_319t1:c.734+30del	NP_000446.1:n.734+30del
XM_005259617.1:c.734+30del	XP_005259674.1:n.734+30del
XM_005259618.3:c.734+30del	XP_005259675.1:n.734+30del
XM_011528209.1:c.512+30del	XP_011526511.1:n.512+30del
XR_936204.1:n.1359+30del
XM_005259617.3:c.734+30del	XP_005259674.1:n.734+30del
XM_011528209.2:c.512+30del	XP_011526511.1:n.512+30del
XR_001753738.2:n.1359+30del
XR_001753739.1:n.1359+30del
XR_001753740.2:n.1359+30del
NM_000455.5:c.734+30del MANE Select	NP_000446.1:n.734+30del