Canonical Allele Identifier: CA2582592935

Gene: STK11

Linked Data

• gnomAD v4: 19-1220538-C-CCCCTCCCGGGCACTCCCTGAGGGCTGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220540_1220567dup , CM000681.2:g.1220540_1220567dup	GRCh38
NC_000019.9:g.1220539_1220566dup , CM000681.1:g.1220539_1220566dup	GRCh37
NC_000019.8:g.1171539_1171566dup	NCBI36
NG_007460.2:g.36134_36161dup , LRG_319:g.36134_36161dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.597+35_598-14dup	ENSP00000490268.2:n.597+35_598-14dup
ENST00000585748.3:c.225+35_226-14dup	ENSP00000477641.2:n.225+35_226-14dup
ENST00000585851.2:c.423+35_424-14dup	ENSP00000467912.2:n.423+35_424-14dup
ENST00000326873.12:c.597+35_598-14dup MANE Select	ENSP00000324856.6:n.597+35_598-14dup
ENST00000652231.1:c.597+35_598-14dup	ENSP00000498804.1:n.597+35_598-14dup
ENST00000326873.11:c.597+35_598-14dup	ENSP00000324856.6:n.597+35_598-14dup
ENST00000585851.1:c.423+35_424-14dup	ENSP00000467912.1:n.423+35_424-14dup
ENST00000586243.5:c.597+35_598-14dup	ENSP00000467240.2:n.597+35_598-14dup
ENST00000586358.5:n.455_482dup
ENST00000589152.5:n.687+35_688-14dup
ENST00000591133.2:n.528_555dup
NM_000455.4:c.597+35_598-14dup , LRG_319t1:c.597+35_598-14dup	NP_000446.1:n.597+35_598-14dup
XM_005259617.1:c.597+35_598-14dup	XP_005259674.1:n.597+35_598-14dup
XM_005259618.3:c.597+35_598-14dup	XP_005259675.1:n.597+35_598-14dup
XM_011528209.1:c.375+35_376-14dup	XP_011526511.1:n.375+35_376-14dup
XR_936204.1:n.1222+35_1223-14dup
XM_005259617.3:c.597+35_598-14dup	XP_005259674.1:n.597+35_598-14dup
XM_011528209.2:c.375+35_376-14dup	XP_011526511.1:n.375+35_376-14dup
XR_001753738.2:n.1222+35_1223-14dup
XR_001753739.1:n.1222+35_1223-14dup
XR_001753740.2:n.1222+35_1223-14dup
NM_000455.5:c.597+35_598-14dup MANE Select	NP_000446.1:n.597+35_598-14dup