Canonical Allele Identifier: CA2813249019

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221476del , CM000681.2:g.1221476del	GRCh38
NC_000019.9:g.1221475del , CM000681.1:g.1221475del	GRCh37
NC_000019.8:g.1172475del	NCBI36
NG_007460.2:g.37070del , LRG_319:g.37070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.862+136del	ENSP00000490268.2:n.862+136del
ENST00000585748.3:c.490+136del	ENSP00000477641.2:n.490+136del
ENST00000585851.2:c.688+136del	ENSP00000467912.2:n.688+136del
ENST00000326873.12:c.862+136del MANE Select	ENSP00000324856.6:n.862+136del
ENST00000652231.1:c.862+136del	ENSP00000498804.1:n.862+136del
ENST00000326873.11:c.862+136del	ENSP00000324856.6:n.862+136del
ENST00000586243.5:c.862+136del	ENSP00000467240.2:n.862+136del
ENST00000586358.5:n.760+136del
ENST00000589152.5:n.1088del
ENST00000591133.2:n.833+136del
NM_000455.4:c.862+136del , LRG_319t1:c.862+136del	NP_000446.1:n.862+136del
XM_005259617.1:c.862+136del	XP_005259674.1:n.862+136del
XM_005259618.3:c.862+136del	XP_005259675.1:n.862+136del
XM_011528209.1:c.640+136del	XP_011526511.1:n.640+136del
XR_936204.1:n.1487+136del
XM_005259617.3:c.862+136del	XP_005259674.1:n.862+136del
XM_011528209.2:c.640+136del	XP_011526511.1:n.640+136del
XR_001753738.2:n.1487+136del
XR_001753739.1:n.1487+136del
XR_001753740.2:n.1487+136del
NM_000455.5:c.862+136del MANE Select	NP_000446.1:n.862+136del