Canonical Allele Identifier: CA402951339

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222006G>A , CM000681.2:g.1222006G>A	GRCh38
NC_000019.9:g.1222005G>A , CM000681.1:g.1222005G>A	GRCh37
NC_000019.8:g.1173005G>A	NCBI36
NG_007460.2:g.37600G>A , LRG_319:g.37600G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.920G>A MANE Select	NP_000446.1:p.Ser307Asn
ENST00000326873.12:c.920G>A MANE Select	ENSP00000324856.6:p.Ser307Asn
NM_000455.4:c.920G>A , LRG_319t1:c.920G>A	NP_000446.1:p.Ser307Asn
ENST00000326873.11:c.920G>A	ENSP00000324856.6:p.Ser307Asn
ENST00000585465.3:c.920G>A	ENSP00000490268.2:p.Ser307Asn
ENST00000585748.3:c.548G>A	ENSP00000477641.2:p.Ser183Asn
ENST00000585851.2:c.746G>A	ENSP00000467912.2:p.Ser249Asn
ENST00000586243.5:c.920G>A	ENSP00000467240.2:p.Ser307Asn
ENST00000589152.5:n.1618G>A
ENST00000591133.2:n.891G>A
ENST00000652231.1:c.920G>A	ENSP00000498804.1:p.Ser307Asn
XM_005259617.1:c.920G>A	XP_005259674.1:p.Ser307Asn
XM_005259617.3:c.920G>A	XP_005259674.1:p.Ser307Asn
XM_005259618.3:c.920G>A	XP_005259675.1:p.Ser307Asn
XM_011528209.1:c.698G>A	XP_011526511.1:p.Ser233Asn
XM_011528209.2:c.698G>A	XP_011526511.1:p.Ser233Asn
XR_001753738.2:n.1726G>A
XR_001753739.1:n.1726G>A
XR_001753740.2:n.1696G>A
XR_936204.1:n.1696G>A