Canonical Allele Identifier: CA402954276

Gene: STK11

Linked Data

• dbSNP Id: rs2145436646
• MyVariant Identifiers: chr19:g.1226636A>G (hg19) ; chr19:g.1226637A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226637A>G , CM000681.2:g.1226637A>G	GRCh38
NC_000019.9:g.1226636A>G , CM000681.1:g.1226636A>G	GRCh37
NC_000019.8:g.1177636A>G	NCBI36
NG_007460.2:g.42231A>G , LRG_319:g.42231A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2893A>G	ENSP00000490268.2:n.*2893A>G
ENST00000585748.3:c.920A>G	ENSP00000477641.2:p.Lys307Arg
ENST00000585851.2:c.1118A>G	ENSP00000467912.2:p.Lys373Arg
ENST00000326873.12:c.1292A>G MANE Select	ENSP00000324856.6:p.Lys431Arg
ENST00000326873.11:c.1292A>G	ENSP00000324856.6:p.Lys431Arg
ENST00000585465.2:n.3025A>G
ENST00000586243.5:c.1289A>G	ENSP00000467240.2:p.Lys430Arg
ENST00000589152.5:n.1990A>G
NM_000455.4:c.1292A>G , LRG_319t1:c.1292A>G	NP_000446.1:p.Lys431Arg
XM_005259617.1:c.1287A>G	XP_005259674.1:p.Gln429=
XM_011528209.1:c.1065A>G	XP_011526511.1:p.Gln355=
XM_005259617.3:c.1287A>G	XP_005259674.1:p.Gln429=
XM_011528209.2:c.1065A>G	XP_011526511.1:p.Gln355=
XR_001753738.2:n.2098A>G
XR_001753740.2:n.2068A>G
NM_000455.5:c.1292A>G MANE Select	NP_000446.1:p.Lys431Arg