Canonical Allele Identifier: CA402953595

Gene: STK11

Linked Data

• ClinVar Variation Id: 2070917
• ClinVar RCV Id: RCV002971515
• dbSNP Id: rs763314442
• MyVariant Identifiers: chr19:g.1226530G>A (hg19) ; chr19:g.1226531G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226531G>A , CM000681.2:g.1226531G>A	GRCh38
NC_000019.9:g.1226530G>A , CM000681.1:g.1226530G>A	GRCh37
NC_000019.8:g.1177530G>A	NCBI36
NG_007460.2:g.42125G>A , LRG_319:g.42125G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2787G>A	ENSP00000490268.2:n.*2787G>A
ENST00000585748.3:c.814G>A	ENSP00000477641.2:p.Glu272Lys
ENST00000585851.2:c.1012G>A	ENSP00000467912.2:p.Glu338Lys
ENST00000326873.12:c.1186G>A MANE Select	ENSP00000324856.6:p.Glu396Lys
ENST00000326873.11:c.1186G>A	ENSP00000324856.6:p.Glu396Lys
ENST00000585465.2:n.2919G>A
ENST00000586243.5:c.1186G>A	ENSP00000467240.2:p.Glu396Lys
ENST00000589152.5:n.1884G>A
NM_000455.4:c.1186G>A , LRG_319t1:c.1186G>A	NP_000446.1:p.Glu396Lys
XM_005259617.1:c.1181G>A	XP_005259674.1:p.Arg394Lys
XM_011528209.1:c.959G>A	XP_011526511.1:p.Arg320Lys
XM_005259617.3:c.1181G>A	XP_005259674.1:p.Arg394Lys
XM_011528209.2:c.959G>A	XP_011526511.1:p.Arg320Lys
XR_001753738.2:n.1992G>A
XR_001753740.2:n.1962G>A
NM_000455.5:c.1186G>A MANE Select	NP_000446.1:p.Glu396Lys