Canonical Allele Identifier: CA402953363

Gene: STK11

Linked Data

• dbSNP Id: rs535449626
• MyVariant Identifiers: chr19:g.1226491C>A (hg19) ; chr19:g.1226492C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226492C>A , CM000681.2:g.1226492C>A	GRCh38
NC_000019.9:g.1226491C>A , CM000681.1:g.1226491C>A	GRCh37
NC_000019.8:g.1177491C>A	NCBI36
NG_007460.2:g.42086C>A , LRG_319:g.42086C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2748C>A	ENSP00000490268.2:n.*2748C>A
ENST00000585748.3:c.775C>A	ENSP00000477641.2:p.Arg259Ser
ENST00000585851.2:c.973C>A	ENSP00000467912.2:p.Arg325Ser
ENST00000326873.12:c.1147C>A MANE Select	ENSP00000324856.6:p.Arg383Ser
ENST00000326873.11:c.1147C>A	ENSP00000324856.6:p.Arg383Ser
ENST00000585465.2:n.2880C>A
ENST00000586243.5:c.1147C>A	ENSP00000467240.2:p.Arg383Ser
ENST00000589152.5:n.1845C>A
NM_000455.4:c.1147C>A , LRG_319t1:c.1147C>A	NP_000446.1:p.Arg383Ser
XM_005259617.1:c.1142C>A	XP_005259674.1:p.Ala381Glu
XM_011528209.1:c.920C>A	XP_011526511.1:p.Ala307Glu
XM_005259617.3:c.1142C>A	XP_005259674.1:p.Ala381Glu
XM_011528209.2:c.920C>A	XP_011526511.1:p.Ala307Glu
XR_001753738.2:n.1953C>A
XR_001753740.2:n.1923C>A
NM_000455.5:c.1147C>A MANE Select	NP_000446.1:p.Arg383Ser