Canonical Allele Identifier: CA2695227882

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219408_1219409dup , CM000681.2:g.1219408_1219409dup	GRCh38
NC_000019.9:g.1219407_1219408dup , CM000681.1:g.1219407_1219408dup	GRCh37
NC_000019.8:g.1170407_1170408dup	NCBI36
NG_007460.2:g.35002_35003dup , LRG_319:g.35002_35003dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.459_460dup	ENSP00000490268.2:p.His154ProfsTer8
ENST00000585748.3:c.87_88dup	ENSP00000477641.2:p.His30ProfsTer8
ENST00000585851.2:c.291-965_291-964dup	ENSP00000467912.2:n.291-965_291-964dup
ENST00000326873.12:c.459_460dup MANE Select	ENSP00000324856.6:p.His154ProfsTer8
ENST00000652231.1:c.459_460dup	ENSP00000498804.1:p.His154ProfsTer8
ENST00000326873.11:c.459_460dup	ENSP00000324856.6:p.His154ProfsTer8
ENST00000585851.1:c.291-965_291-964dup	ENSP00000467912.1:n.291-965_291-964dup
ENST00000586243.5:c.459_460dup	ENSP00000467240.2:p.His154ProfsTer8
ENST00000586358.5:n.282_283dup
ENST00000589152.5:n.549_550dup
NM_000455.4:c.459_460dup , LRG_319t1:c.459_460dup	NP_000446.1:p.His154ProfsTer8
XM_005259617.1:c.459_460dup	XP_005259674.1:p.His154ProfsTer8
XM_005259618.3:c.459_460dup	XP_005259675.1:p.His154ProfsTer8
XM_011528209.1:c.237_238dup	XP_011526511.1:p.His80ProfsTer8
XR_936204.1:n.1084_1085dup
XM_005259617.3:c.459_460dup	XP_005259674.1:p.His154ProfsTer8
XM_011528209.2:c.237_238dup	XP_011526511.1:p.His80ProfsTer8
XR_001753738.2:n.1084_1085dup
XR_001753739.1:n.1084_1085dup
XR_001753740.2:n.1084_1085dup
NM_000455.5:c.459_460dup MANE Select	NP_000446.1:p.His154ProfsTer8