Canonical Allele Identifier: CA2582592088

Gene: STK11

Linked Data

• gnomAD v4: 19-1219423-C-CGGGGCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219427_1219433dup , CM000681.2:g.1219427_1219433dup	GRCh38
NC_000019.9:g.1219426_1219432dup , CM000681.1:g.1219426_1219432dup	GRCh37
NC_000019.8:g.1170426_1170432dup	NCBI36
NG_007460.2:g.35021_35027dup , LRG_319:g.35021_35027dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.464+14_464+20dup	ENSP00000490268.2:n.464+14_464+20dup
ENST00000585748.3:c.92+14_92+20dup	ENSP00000477641.2:n.92+14_92+20dup
ENST00000585851.2:c.291-946_291-940dup	ENSP00000467912.2:n.291-946_291-940dup
ENST00000326873.12:c.464+14_464+20dup MANE Select	ENSP00000324856.6:n.464+14_464+20dup
ENST00000652231.1:c.464+14_464+20dup	ENSP00000498804.1:n.464+14_464+20dup
ENST00000326873.11:c.464+14_464+20dup	ENSP00000324856.6:n.464+14_464+20dup
ENST00000585851.1:c.291-946_291-940dup	ENSP00000467912.1:n.291-946_291-940dup
ENST00000586243.5:c.464+14_464+20dup	ENSP00000467240.2:n.464+14_464+20dup
ENST00000586358.5:n.287+14_287+20dup
ENST00000589152.5:n.554+14_554+20dup
NM_000455.4:c.464+14_464+20dup , LRG_319t1:c.464+14_464+20dup	NP_000446.1:n.464+14_464+20dup
XM_005259617.1:c.464+14_464+20dup	XP_005259674.1:n.464+14_464+20dup
XM_005259618.3:c.464+14_464+20dup	XP_005259675.1:n.464+14_464+20dup
XM_011528209.1:c.242+14_242+20dup	XP_011526511.1:n.242+14_242+20dup
XR_936204.1:n.1089+14_1089+20dup
XM_005259617.3:c.464+14_464+20dup	XP_005259674.1:n.464+14_464+20dup
XM_011528209.2:c.242+14_242+20dup	XP_011526511.1:n.242+14_242+20dup
XR_001753738.2:n.1089+14_1089+20dup
XR_001753739.1:n.1089+14_1089+20dup
XR_001753740.2:n.1089+14_1089+20dup
NM_000455.5:c.464+14_464+20dup MANE Select	NP_000446.1:n.464+14_464+20dup