Canonical Allele Identifier: CA2317590127

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220952_1220955delinsCCCT , CM000681.2:g.1220952_1220955delinsCCCT	GRCh38
NC_000019.9:g.1220951_1220954delinsCCCT , CM000681.1:g.1220951_1220954delinsCCCT	GRCh37
NC_000019.8:g.1171951_1171954delinsCCCT	NCBI36
NG_007460.2:g.36546_36549delinsCCCT , LRG_319:g.36546_36549delinsCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.734+235_734+238delinsCCCT	ENSP00000490268.2:n.734+235_734+238delinsCCCT
ENST00000585748.3:c.362+235_362+238delinsCCCT	ENSP00000477641.2:n.362+235_362+238delinsCCCT
ENST00000585851.2:c.560+235_560+238delinsCCCT	ENSP00000467912.2:n.560+235_560+238delinsCCCT
ENST00000326873.12:c.734+235_734+238delinsCCCT MANE Select	ENSP00000324856.6:n.734+235_734+238delinsCCCT
ENST00000652231.1:c.734+235_734+238delinsCCCT	ENSP00000498804.1:n.734+235_734+238delinsCCCT
ENST00000326873.11:c.734+235_734+238delinsCCCT	ENSP00000324856.6:n.734+235_734+238delinsCCCT
ENST00000586243.5:c.734+235_734+238delinsCCCT	ENSP00000467240.2:n.734+235_734+238delinsCCCT
ENST00000586358.5:n.632+235_632+238delinsCCCT
ENST00000589152.5:n.824+235_824+238delinsCCCT
ENST00000591133.2:n.705+235_705+238delinsCCCT
NM_000455.4:c.734+235_734+238delinsCCCT , LRG_319t1:c.734+235_734+238delinsCCCT	NP_000446.1:n.734+235_734+238delinsCCCT
XM_005259617.1:c.734+235_734+238delinsCCCT	XP_005259674.1:n.734+235_734+238delinsCCCT
XM_005259618.3:c.734+235_734+238delinsCCCT	XP_005259675.1:n.734+235_734+238delinsCCCT
XM_011528209.1:c.512+235_512+238delinsCCCT	XP_011526511.1:n.512+235_512+238delinsCCCT
XR_936204.1:n.1359+235_1359+238delinsCCCT
XM_005259617.3:c.734+235_734+238delinsCCCT	XP_005259674.1:n.734+235_734+238delinsCCCT
XM_011528209.2:c.512+235_512+238delinsCCCT	XP_011526511.1:n.512+235_512+238delinsCCCT
XR_001753738.2:n.1359+235_1359+238delinsCCCT
XR_001753739.1:n.1359+235_1359+238delinsCCCT
XR_001753740.2:n.1359+235_1359+238delinsCCCT
NM_000455.5:c.734+235_734+238delinsCCCT MANE Select	NP_000446.1:n.734+235_734+238delinsCCCT