Canonical Allele Identifier: CA16608853

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226656G>A , CM000681.2:g.1226656G>A	GRCh38
NC_000019.9:g.1226655G>A , CM000681.1:g.1226655G>A	GRCh37
NC_000019.8:g.1177655G>A	NCBI36
NG_007460.2:g.42250G>A , LRG_319:g.42250G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.*9G>A MANE Select	NP_000446.1:n.*9G>A
ENST00000326873.12:c.*9G>A MANE Select	ENSP00000324856.6:n.*9G>A
NM_000455.4:c.*9G>A , LRG_319t1:c.*9G>A	NP_000446.1:n.*9G>A
ENST00000326873.11:c.*9G>A	ENSP00000324856.6:n.*9G>A
ENST00000585465.2:n.3044G>A
ENST00000585465.3:c.*2912G>A	ENSP00000490268.2:n.*2912G>A
ENST00000585748.3:c.*9G>A	ENSP00000477641.2:n.*9G>A
ENST00000585851.2:c.*9G>A	ENSP00000467912.2:n.*9G>A
ENST00000586243.5:c.*9G>A	ENSP00000467240.2:n.*9G>A
ENST00000589152.5:n.2009G>A
XM_005259617.1:c.1306G>A	XP_005259674.1:p.Ala436Thr
XM_005259617.3:c.1306G>A	XP_005259674.1:p.Ala436Thr
XM_011528209.1:c.1084G>A	XP_011526511.1:p.Ala362Thr
XM_011528209.2:c.1084G>A	XP_011526511.1:p.Ala362Thr
XR_001753738.2:n.2117G>A
XR_001753740.2:n.2087G>A