Canonical Allele Identifier: CA402947617

Gene: STK11

Linked Data

• ClinVar Variation Id: 856981
• ClinVar RCV Id: RCV001062565
• dbSNP Id: rs1599924529
• MyVariant Identifiers: chr19:g.1218416G>C (hg19) ; chr19:g.1218417G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218417G>C , CM000681.2:g.1218417G>C	GRCh38
NC_000019.9:g.1218416G>C , CM000681.1:g.1218416G>C	GRCh37
NC_000019.8:g.1169416G>C	NCBI36
NG_007460.2:g.34011G>C , LRG_319:g.34011G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291G>C	ENSP00000490268.2:p.Lys97Asn
ENST00000585748.3:c.-82G>C	ENSP00000477641.2:n.-82G>C
ENST00000585851.2:c.291-1956G>C	ENSP00000467912.2:n.291-1956G>C
ENST00000326873.12:c.291G>C MANE Select	ENSP00000324856.6:p.Lys97Asn
ENST00000652231.1:c.291G>C	ENSP00000498804.1:p.Lys97Asn
ENST00000326873.11:c.291G>C	ENSP00000324856.6:p.Lys97Asn
ENST00000585748.2:c.-82G>C	ENSP00000477641.1:n.-82G>C
ENST00000585851.1:c.291-1956G>C	ENSP00000467912.1:n.291-1956G>C
ENST00000586243.5:c.291G>C	ENSP00000467240.2:p.Lys97Asn
ENST00000586358.5:n.114G>C
ENST00000589152.5:n.381G>C
ENST00000593219.5:c.*116G>C	ENSP00000466610.1:n.*116G>C
NM_000455.4:c.291G>C , LRG_319t1:c.291G>C	NP_000446.1:p.Lys97Asn
XM_005259617.1:c.291G>C	XP_005259674.1:p.Lys97Asn
XM_005259618.3:c.291G>C	XP_005259675.1:p.Lys97Asn
XM_011528209.1:c.69G>C	XP_011526511.1:p.Trp23Cys
XR_936204.1:n.916G>C
XM_005259617.3:c.291G>C	XP_005259674.1:p.Lys97Asn
XM_011528209.2:c.69G>C	XP_011526511.1:p.Trp23Cys
XR_001753738.2:n.916G>C
XR_001753739.1:n.916G>C
XR_001753740.2:n.916G>C
NM_000455.5:c.291G>C MANE Select	NP_000446.1:p.Lys97Asn