Canonical Allele Identifier: CA2576546335

Gene: STK11

Linked Data

• gnomAD v4: 19-1220273-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220276del , CM000681.2:g.1220276del	GRCh38
NC_000019.9:g.1220275del , CM000681.1:g.1220275del	GRCh37
NC_000019.8:g.1171275del	NCBI36
NG_007460.2:g.35870del , LRG_319:g.35870del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.465-97del	ENSP00000490268.2:n.465-97del
ENST00000585748.3:c.93-97del	ENSP00000477641.2:n.93-97del
ENST00000585851.2:c.291-97del	ENSP00000467912.2:n.291-97del
ENST00000326873.12:c.465-97del MANE Select	ENSP00000324856.6:n.465-97del
ENST00000652231.1:c.465-97del	ENSP00000498804.1:n.465-97del
ENST00000326873.11:c.465-97del	ENSP00000324856.6:n.465-97del
ENST00000585851.1:c.291-97del	ENSP00000467912.1:n.291-97del
ENST00000586243.5:c.465-97del	ENSP00000467240.2:n.465-97del
ENST00000586358.5:n.288-97del
ENST00000589152.5:n.555-97del
ENST00000591133.2:n.264del
NM_000455.4:c.465-97del , LRG_319t1:c.465-97del	NP_000446.1:n.465-97del
XM_005259617.1:c.465-97del	XP_005259674.1:n.465-97del
XM_005259618.3:c.465-97del	XP_005259675.1:n.465-97del
XM_011528209.1:c.243-97del	XP_011526511.1:n.243-97del
XR_936204.1:n.1090-97del
XM_005259617.3:c.465-97del	XP_005259674.1:n.465-97del
XM_011528209.2:c.243-97del	XP_011526511.1:n.243-97del
XR_001753738.2:n.1090-97del
XR_001753739.1:n.1090-97del
XR_001753740.2:n.1090-97del
NM_000455.5:c.465-97del MANE Select	NP_000446.1:n.465-97del