Canonical Allele Identifier: CA402951669

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223065G>A , CM000681.2:g.1223065G>A	GRCh38
NC_000019.9:g.1223064G>A , CM000681.1:g.1223064G>A	GRCh37
NC_000019.8:g.1174064G>A	NCBI36
NG_007460.2:g.38659G>A , LRG_319:g.38659G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1001G>A MANE Select	NP_000446.1:p.Ser334Asn
ENST00000326873.12:c.1001G>A MANE Select	ENSP00000324856.6:p.Ser334Asn
NM_000455.4:c.1001G>A , LRG_319t1:c.1001G>A	NP_000446.1:p.Ser334Asn
ENST00000326873.11:c.1001G>A	ENSP00000324856.6:p.Ser334Asn
ENST00000585465.3:c.1001G>A	ENSP00000490268.2:p.Ser334Asn
ENST00000585748.3:c.629G>A	ENSP00000477641.2:p.Ser210Asn
ENST00000585851.2:c.827G>A	ENSP00000467912.2:p.Ser276Asn
ENST00000586243.5:c.1001G>A	ENSP00000467240.2:p.Ser334Asn
ENST00000589152.5:n.1699G>A
ENST00000591133.2:n.972G>A
ENST00000652231.1:c.1001G>A	ENSP00000498804.1:p.Ser334Asn
XM_005259617.1:c.1001G>A	XP_005259674.1:p.Ser334Asn
XM_005259617.3:c.1001G>A	XP_005259674.1:p.Ser334Asn
XM_005259618.3:c.1001G>A	XP_005259675.1:p.Ser334Asn
XM_011528209.1:c.779G>A	XP_011526511.1:p.Ser260Asn
XM_011528209.2:c.779G>A	XP_011526511.1:p.Ser260Asn
XR_001753738.2:n.1807G>A
XR_001753739.1:n.1807G>A
XR_001753740.2:n.1777G>A
XR_936204.1:n.1777G>A