Canonical Allele Identifier: CA2582591348

Gene: STK11

Linked Data

• gnomAD v4: 19-1206876-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206877_1206878del , CM000681.2:g.1206877_1206878del	GRCh38
NC_000019.9:g.1206876_1206877del , CM000681.1:g.1206876_1206877del	GRCh37
NC_000019.8:g.1157876_1157877del	NCBI36
NG_007460.2:g.22471_22472del , LRG_319:g.22471_22472del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-37_-36del	ENSP00000490268.2:n.-37_-36del
ENST00000585748.3:c.-82-11540_-82-11539del	ENSP00000477641.2:n.-82-11540_-82-11539del
ENST00000585851.2:c.-37_-36del	ENSP00000467912.2:n.-37_-36del
ENST00000326873.12:c.-37_-36del MANE Select	ENSP00000324856.6:n.-37_-36del
ENST00000652231.1:c.-37_-36del	ENSP00000498804.1:n.-37_-36del
ENST00000326873.11:c.-37_-36del	ENSP00000324856.6:n.-37_-36del
ENST00000585748.2:c.-82-11540_-82-11539del	ENSP00000477641.1:n.-82-11540_-82-11539del
ENST00000585851.1:c.-37_-36del	ENSP00000467912.1:n.-37_-36del
ENST00000586243.5:c.-37_-36del	ENSP00000467240.2:n.-37_-36del
ENST00000589152.5:n.54_55del
ENST00000593219.5:c.-37_-36del	ENSP00000466610.1:n.-37_-36del
NM_000455.4:c.-37_-36del , LRG_319t1:c.-37_-36del	NP_000446.1:n.-37_-36del
XM_005259617.1:c.-37_-36del	XP_005259674.1:n.-37_-36del
XM_005259618.3:c.-37_-36del	XP_005259675.1:n.-37_-36del
XM_011528209.1:c.-390_-389del	XP_011526511.1:n.-390_-389del
XR_936204.1:n.589_590del
XM_005259617.3:c.-37_-36del	XP_005259674.1:n.-37_-36del
XM_011528209.2:c.-390_-389del	XP_011526511.1:n.-390_-389del
XR_001753738.2:n.589_590del
XR_001753739.1:n.589_590del
XR_001753740.2:n.589_590del
NM_000455.5:c.-37_-36del MANE Select	NP_000446.1:n.-37_-36del