Canonical Allele Identifier: CA2813238372

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220840_1220841insGGGGA , CM000681.2:g.1220840_1220841insGGGGA	GRCh38
NC_000019.9:g.1220839_1220840insGGGGA , CM000681.1:g.1220839_1220840insGGGGA	GRCh37
NC_000019.8:g.1171839_1171840insGGGGA	NCBI36
NG_007460.2:g.36434_36435insGGGGA , LRG_319:g.36434_36435insGGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.734+123_734+124insGGGGA	ENSP00000490268.2:n.734+123_734+124insGGGGA
ENST00000585748.3:c.362+123_362+124insGGGGA	ENSP00000477641.2:n.362+123_362+124insGGGGA
ENST00000585851.2:c.560+123_560+124insGGGGA	ENSP00000467912.2:n.560+123_560+124insGGGGA
ENST00000326873.12:c.734+123_734+124insGGGGA MANE Select	ENSP00000324856.6:n.734+123_734+124insGGGGA
ENST00000652231.1:c.734+123_734+124insGGGGA	ENSP00000498804.1:n.734+123_734+124insGGGGA
ENST00000326873.11:c.734+123_734+124insGGGGA	ENSP00000324856.6:n.734+123_734+124insGGGGA
ENST00000586243.5:c.734+123_734+124insGGGGA	ENSP00000467240.2:n.734+123_734+124insGGGGA
ENST00000586358.5:n.632+123_632+124insGGGGA
ENST00000589152.5:n.824+123_824+124insGGGGA
ENST00000591133.2:n.705+123_705+124insGGGGA
NM_000455.4:c.734+123_734+124insGGGGA , LRG_319t1:c.734+123_734+124insGGGGA	NP_000446.1:n.734+123_734+124insGGGGA
XM_005259617.1:c.734+123_734+124insGGGGA	XP_005259674.1:n.734+123_734+124insGGGGA
XM_005259618.3:c.734+123_734+124insGGGGA	XP_005259675.1:n.734+123_734+124insGGGGA
XM_011528209.1:c.512+123_512+124insGGGGA	XP_011526511.1:n.512+123_512+124insGGGGA
XR_936204.1:n.1359+123_1359+124insGGGGA
XM_005259617.3:c.734+123_734+124insGGGGA	XP_005259674.1:n.734+123_734+124insGGGGA
XM_011528209.2:c.512+123_512+124insGGGGA	XP_011526511.1:n.512+123_512+124insGGGGA
XR_001753738.2:n.1359+123_1359+124insGGGGA
XR_001753739.1:n.1359+123_1359+124insGGGGA
XR_001753740.2:n.1359+123_1359+124insGGGGA
NM_000455.5:c.734+123_734+124insGGGGA MANE Select	NP_000446.1:n.734+123_734+124insGGGGA