Canonical Allele Identifier: CA16608838

Gene: STK11

Linked Data

• ClinVar Variation Id: 392308
• ClinVar RCV Id: RCV000434265 ; RCV001362693 ; RCV002374723
• dbSNP Id: rs1057524439
• MyVariant Identifiers: chr19:g.1221954T>C (hg19) ; chr19:g.1221955T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221955T>C , CM000681.2:g.1221955T>C	GRCh38
NC_000019.9:g.1221954T>C , CM000681.1:g.1221954T>C	GRCh37
NC_000019.8:g.1172954T>C	NCBI36
NG_007460.2:g.37549T>C , LRG_319:g.37549T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.869T>C	ENSP00000490268.2:p.Leu290Pro
ENST00000585748.3:c.497T>C	ENSP00000477641.2:p.Leu166Pro
ENST00000585851.2:c.695T>C	ENSP00000467912.2:p.Leu232Pro
ENST00000326873.12:c.869T>C MANE Select	ENSP00000324856.6:p.Leu290Pro
ENST00000652231.1:c.869T>C	ENSP00000498804.1:p.Leu290Pro
ENST00000326873.11:c.869T>C	ENSP00000324856.6:p.Leu290Pro
ENST00000586243.5:c.869T>C	ENSP00000467240.2:p.Leu290Pro
ENST00000586358.5:n.767T>C
ENST00000589152.5:n.1567T>C
ENST00000591133.2:n.840T>C
NM_000455.4:c.869T>C , LRG_319t1:c.869T>C	NP_000446.1:p.Leu290Pro
XM_005259617.1:c.869T>C	XP_005259674.1:p.Leu290Pro
XM_005259618.3:c.869T>C	XP_005259675.1:p.Leu290Pro
XM_011528209.1:c.647T>C	XP_011526511.1:p.Leu216Pro
XR_936204.1:n.1645T>C
XM_005259617.3:c.869T>C	XP_005259674.1:p.Leu290Pro
XM_011528209.2:c.647T>C	XP_011526511.1:p.Leu216Pro
XR_001753738.2:n.1675T>C
XR_001753739.1:n.1675T>C
XR_001753740.2:n.1645T>C
NM_000455.5:c.869T>C MANE Select	NP_000446.1:p.Leu290Pro