Canonical Allele Identifier: CA402953768

Gene: STK11

Linked Data

• dbSNP Id: rs2145436259
• MyVariant Identifiers: chr19:g.1226558G>A (hg19) ; chr19:g.1226559G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226559G>A , CM000681.2:g.1226559G>A	GRCh38
NC_000019.9:g.1226558G>A , CM000681.1:g.1226558G>A	GRCh37
NC_000019.8:g.1177558G>A	NCBI36
NG_007460.2:g.42153G>A , LRG_319:g.42153G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2815G>A	ENSP00000490268.2:n.*2815G>A
ENST00000585748.3:c.842G>A	ENSP00000477641.2:p.Arg281Lys
ENST00000585851.2:c.1040G>A	ENSP00000467912.2:p.Arg347Lys
ENST00000326873.12:c.1214G>A MANE Select	ENSP00000324856.6:p.Arg405Lys
ENST00000326873.11:c.1214G>A	ENSP00000324856.6:p.Arg405Lys
ENST00000585465.2:n.2947G>A
ENST00000586243.5:c.1214G>A	ENSP00000467240.2:p.Arg405Lys
ENST00000589152.5:n.1912G>A
NM_000455.4:c.1214G>A , LRG_319t1:c.1214G>A	NP_000446.1:p.Arg405Lys
XM_005259617.1:c.1209G>A	XP_005259674.1:p.Gln403=
XM_011528209.1:c.987G>A	XP_011526511.1:p.Gln329=
XM_005259617.3:c.1209G>A	XP_005259674.1:p.Gln403=
XM_011528209.2:c.987G>A	XP_011526511.1:p.Gln329=
XR_001753738.2:n.2020G>A
XR_001753740.2:n.1990G>A
NM_000455.5:c.1214G>A MANE Select	NP_000446.1:p.Arg405Lys