Canonical Allele Identifier: CA402954281

Gene: STK11

Linked Data

• ClinVar Variation Id: 1332544
• ClinVar RCV Id: RCV001805590
• dbSNP Id: rs2145436646
• MyVariant Identifiers: chr19:g.1226636A>C (hg19) ; chr19:g.1226637A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2893A>C	ENSP00000490268.2:n.*2893A>C
ENST00000585748.3:c.920A>C	ENSP00000477641.2:p.Lys307Thr
ENST00000585851.2:c.1118A>C	ENSP00000467912.2:p.Lys373Thr
ENST00000326873.12:c.1292A>C MANE Select	ENSP00000324856.6:p.Lys431Thr
ENST00000326873.11:c.1292A>C	ENSP00000324856.6:p.Lys431Thr
ENST00000585465.2:n.3025A>C
ENST00000586243.5:c.1289A>C	ENSP00000467240.2:p.Lys430Thr
ENST00000589152.5:n.1990A>C
NM_000455.4:c.1292A>C , LRG_319t1:c.1292A>C	NP_000446.1:p.Lys431Thr
XM_005259617.1:c.1287A>C	XP_005259674.1:p.Gln429His
XM_011528209.1:c.1065A>C	XP_011526511.1:p.Gln355His
XM_005259617.3:c.1287A>C	XP_005259674.1:p.Gln429His
XM_011528209.2:c.1065A>C	XP_011526511.1:p.Gln355His
XR_001753738.2:n.2098A>C
XR_001753740.2:n.2068A>C
NM_000455.5:c.1292A>C MANE Select	NP_000446.1:p.Lys431Thr