Canonical Allele Identifier: CA2695227887

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221303_1221307dup , CM000681.2:g.1221303_1221307dup	GRCh38
NC_000019.9:g.1221302_1221306dup , CM000681.1:g.1221302_1221306dup	GRCh37
NC_000019.8:g.1172302_1172306dup	NCBI36
NG_007460.2:g.36897_36901dup , LRG_319:g.36897_36901dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.825_829dup	ENSP00000490268.2:p.Asp277GlyfsTer12
ENST00000585748.3:c.453_457dup	ENSP00000477641.2:p.Asp153GlyfsTer12
ENST00000585851.2:c.651_655dup	ENSP00000467912.2:p.Asp219GlyfsTer12
ENST00000326873.12:c.825_829dup MANE Select	ENSP00000324856.6:p.Asp277GlyfsTer12
ENST00000652231.1:c.825_829dup	ENSP00000498804.1:p.Asp277GlyfsTer12
ENST00000326873.11:c.825_829dup	ENSP00000324856.6:p.Asp277GlyfsTer12
ENST00000586243.5:c.825_829dup	ENSP00000467240.2:p.Asp277GlyfsTer12
ENST00000586358.5:n.723_727dup
ENST00000589152.5:n.915_919dup
ENST00000591133.2:n.796_800dup
NM_000455.4:c.825_829dup , LRG_319t1:c.825_829dup	NP_000446.1:p.Asp277GlyfsTer12
XM_005259617.1:c.825_829dup	XP_005259674.1:p.Asp277GlyfsTer12
XM_005259618.3:c.825_829dup	XP_005259675.1:p.Asp277GlyfsTer12
XM_011528209.1:c.603_607dup	XP_011526511.1:p.Asp203GlyfsTer12
XR_936204.1:n.1450_1454dup
XM_005259617.3:c.825_829dup	XP_005259674.1:p.Asp277GlyfsTer12
XM_011528209.2:c.603_607dup	XP_011526511.1:p.Asp203GlyfsTer12
XR_001753738.2:n.1450_1454dup
XR_001753739.1:n.1450_1454dup
XR_001753740.2:n.1450_1454dup
NM_000455.5:c.825_829dup MANE Select	NP_000446.1:p.Asp277GlyfsTer12