Canonical Allele Identifier: CA402954113

Gene: STK11

Linked Data

• ClinVar Variation Id: 2561035
• ClinVar RCV Id: RCV003300757
• dbSNP Id: rs2145436508
• MyVariant Identifiers: chr19:g.1226609G>C (hg19) ; chr19:g.1226610G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226610G>C , CM000681.2:g.1226610G>C	GRCh38
NC_000019.9:g.1226609G>C , CM000681.1:g.1226609G>C	GRCh37
NC_000019.8:g.1177609G>C	NCBI36
NG_007460.2:g.42204G>C , LRG_319:g.42204G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2866G>C	ENSP00000490268.2:n.*2866G>C
ENST00000585748.3:c.893G>C	ENSP00000477641.2:p.Ser298Thr
ENST00000585851.2:c.1091G>C	ENSP00000467912.2:p.Ser364Thr
ENST00000326873.12:c.1265G>C MANE Select	ENSP00000324856.6:p.Ser422Thr
ENST00000326873.11:c.1265G>C	ENSP00000324856.6:p.Ser422Thr
ENST00000585465.2:n.2998G>C
ENST00000586243.5:c.1262G>C	ENSP00000467240.2:p.Ser421Thr
ENST00000589152.5:n.1963G>C
NM_000455.4:c.1265G>C , LRG_319t1:c.1265G>C	NP_000446.1:p.Ser422Thr
XM_005259617.1:c.1260G>C	XP_005259674.1:p.Gln420His
XM_011528209.1:c.1038G>C	XP_011526511.1:p.Gln346His
XM_005259617.3:c.1260G>C	XP_005259674.1:p.Gln420His
XM_011528209.2:c.1038G>C	XP_011526511.1:p.Gln346His
XR_001753738.2:n.2071G>C
XR_001753740.2:n.2041G>C
NM_000455.5:c.1265G>C MANE Select	NP_000446.1:p.Ser422Thr