Canonical Allele Identifier: CA2582591110

Gene: STK11

Linked Data

• gnomAD v4: 19-1206782-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206786del , CM000681.2:g.1206786del	GRCh38
NC_000019.9:g.1206785del , CM000681.1:g.1206785del	GRCh37
NC_000019.8:g.1157785del	NCBI36
NG_007460.2:g.22380del , LRG_319:g.22380del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-128del	ENSP00000490268.2:n.-128del
ENST00000585748.3:c.-82-11631del	ENSP00000477641.2:n.-82-11631del
ENST00000326873.12:c.-128del MANE Select	ENSP00000324856.6:n.-128del
ENST00000652231.1:c.-128del	ENSP00000498804.1:n.-128del
ENST00000326873.11:c.-128del	ENSP00000324856.6:n.-128del
ENST00000585748.2:c.-82-11631del	ENSP00000477641.1:n.-82-11631del
ENST00000586243.5:c.-128del	ENSP00000467240.2:n.-128del
NM_000455.4:c.-128del , LRG_319t1:c.-128del	NP_000446.1:n.-128del
XM_005259617.1:c.-128del	XP_005259674.1:n.-128del
XM_005259618.3:c.-128del	XP_005259675.1:n.-128del
XM_011528209.1:c.-481del	XP_011526511.1:n.-481del
XR_936204.1:n.498del
XM_005259617.3:c.-128del	XP_005259674.1:n.-128del
XM_011528209.2:c.-481del	XP_011526511.1:n.-481del
XR_001753738.2:n.498del
XR_001753739.1:n.498del
XR_001753740.2:n.498del
NM_000455.5:c.-128del MANE Select	NP_000446.1:n.-128del