Canonical Allele Identifier: CA402953097

Gene: STK11

Linked Data

• ClinVar Variation Id: 2451995
• ClinVar RCV Id: RCV003187691 ; RCV003779546
• dbSNP Id: rs1568716651
• MyVariant Identifiers: chr19:g.1226453G>C (hg19) ; chr19:g.1226454G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226454G>C , CM000681.2:g.1226454G>C	GRCh38
NC_000019.9:g.1226453G>C , CM000681.1:g.1226453G>C	GRCh37
NC_000019.8:g.1177453G>C	NCBI36
NG_007460.2:g.42048G>C , LRG_319:g.42048G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2710G>C	ENSP00000490268.2:n.*2710G>C
ENST00000585748.3:c.737G>C	ENSP00000477641.2:p.Gly246Ala
ENST00000585851.2:c.935G>C	ENSP00000467912.2:p.Gly312Ala
ENST00000326873.12:c.1109G>C MANE Select	ENSP00000324856.6:p.Gly370Ala
ENST00000326873.11:c.1109G>C	ENSP00000324856.6:p.Gly370Ala
ENST00000585465.2:n.2842G>C
ENST00000586243.5:c.1109G>C	ENSP00000467240.2:p.Gly370Ala
ENST00000589152.5:n.1807G>C
NM_000455.4:c.1109G>C , LRG_319t1:c.1109G>C	NP_000446.1:p.Gly370Ala
XM_005259617.1:c.1109-5G>C	XP_005259674.1:n.1109-5G>C
XM_011528209.1:c.887-5G>C	XP_011526511.1:n.887-5G>C
XM_005259617.3:c.1109-5G>C	XP_005259674.1:n.1109-5G>C
XM_011528209.2:c.887-5G>C	XP_011526511.1:n.887-5G>C
XR_001753738.2:n.1915G>C
XR_001753740.2:n.1885G>C
NM_000455.5:c.1109G>C MANE Select	NP_000446.1:p.Gly370Ala