Canonical Allele Identifier: CA2543636019

Gene: STK11

Linked Data

• gnomAD v4: 19-1206853-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206855dup , CM000681.2:g.1206855dup	GRCh38
NC_000019.9:g.1206854dup , CM000681.1:g.1206854dup	GRCh37
NC_000019.8:g.1157854dup	NCBI36
NG_007460.2:g.22449dup , LRG_319:g.22449dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.-59dup	ENSP00000490268.2:n.-59dup
ENST00000585748.3:c.-82-11562dup	ENSP00000477641.2:n.-82-11562dup
ENST00000326873.12:c.-59dup MANE Select	ENSP00000324856.6:n.-59dup
ENST00000652231.1:c.-59dup	ENSP00000498804.1:n.-59dup
ENST00000326873.11:c.-59dup	ENSP00000324856.6:n.-59dup
ENST00000585748.2:c.-82-11562dup	ENSP00000477641.1:n.-82-11562dup
ENST00000586243.5:c.-59dup	ENSP00000467240.2:n.-59dup
ENST00000589152.5:n.32dup
ENST00000593219.5:c.-59dup	ENSP00000466610.1:n.-59dup
NM_000455.4:c.-59dup , LRG_319t1:c.-59dup	NP_000446.1:n.-59dup
XM_005259617.1:c.-59dup	XP_005259674.1:n.-59dup
XM_005259618.3:c.-59dup	XP_005259675.1:n.-59dup
XM_011528209.1:c.-412dup	XP_011526511.1:n.-412dup
XR_936204.1:n.567dup
XM_005259617.3:c.-59dup	XP_005259674.1:n.-59dup
XM_011528209.2:c.-412dup	XP_011526511.1:n.-412dup
XR_001753738.2:n.567dup
XR_001753739.1:n.567dup
XR_001753740.2:n.567dup
NM_000455.5:c.-59dup MANE Select	NP_000446.1:n.-59dup