Canonical Allele Identifier: CA783334211

Gene: STK11

Linked Data

• dbSNP Id: rs1191311796
• gnomAD v3: 19-1220320-CCT-C
• gnomAD v4: 19-1220320-CCT-C
• MyVariant Identifiers: chr19:g.1220320_1220321del (hg19) ; chr19:g.1220321_1220322del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220321_1220322del , CM000681.2:g.1220321_1220322del	GRCh38
NC_000019.9:g.1220320_1220321del , CM000681.1:g.1220320_1220321del	GRCh37
NC_000019.8:g.1171320_1171321del	NCBI36
NG_007460.2:g.35915_35916del , LRG_319:g.35915_35916del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.465-52_465-51del	ENSP00000490268.2:n.465-52_465-51del
ENST00000585748.3:c.93-52_93-51del	ENSP00000477641.2:n.93-52_93-51del
ENST00000585851.2:c.291-52_291-51del	ENSP00000467912.2:n.291-52_291-51del
ENST00000326873.12:c.465-52_465-51del MANE Select	ENSP00000324856.6:n.465-52_465-51del
ENST00000652231.1:c.465-52_465-51del	ENSP00000498804.1:n.465-52_465-51del
ENST00000326873.11:c.465-52_465-51del	ENSP00000324856.6:n.465-52_465-51del
ENST00000585851.1:c.291-52_291-51del	ENSP00000467912.1:n.291-52_291-51del
ENST00000586243.5:c.465-52_465-51del	ENSP00000467240.2:n.465-52_465-51del
ENST00000586358.5:n.288-52_288-51del
ENST00000589152.5:n.555-52_555-51del
ENST00000591133.2:n.309_310del
NM_000455.4:c.465-52_465-51del , LRG_319t1:c.465-52_465-51del	NP_000446.1:n.465-52_465-51del
XM_005259617.1:c.465-52_465-51del	XP_005259674.1:n.465-52_465-51del
XM_005259618.3:c.465-52_465-51del	XP_005259675.1:n.465-52_465-51del
XM_011528209.1:c.243-52_243-51del	XP_011526511.1:n.243-52_243-51del
XR_936204.1:n.1090-52_1090-51del
XM_005259617.3:c.465-52_465-51del	XP_005259674.1:n.465-52_465-51del
XM_011528209.2:c.243-52_243-51del	XP_011526511.1:n.243-52_243-51del
XR_001753738.2:n.1090-52_1090-51del
XR_001753739.1:n.1090-52_1090-51del
XR_001753740.2:n.1090-52_1090-51del
NM_000455.5:c.465-52_465-51del MANE Select	NP_000446.1:n.465-52_465-51del