Canonical Allele Identifier: CA023303

Gene: STK11

Linked Data

• ClinVar Variation Id: 185022
• ClinVar RCV Id: RCV000164375 ; RCV000228218 ; RCV003467293
• dbSNP Id: rs121913322
• gnomAD v4: 19-1221320-C-G
• MyVariant Identifiers: chr19:g.1221319C>G (hg19) ; chr19:g.1221320C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221320C>G , CM000681.2:g.1221320C>G	GRCh38
NC_000019.9:g.1221319C>G , CM000681.1:g.1221319C>G	GRCh37
NC_000019.8:g.1172319C>G	NCBI36
NG_007460.2:g.36914C>G , LRG_319:g.36914C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.842C>G	ENSP00000490268.2:p.Pro281Arg
ENST00000585748.3:c.470C>G	ENSP00000477641.2:p.Pro157Arg
ENST00000585851.2:c.668C>G	ENSP00000467912.2:p.Pro223Arg
ENST00000326873.12:c.842C>G MANE Select	ENSP00000324856.6:p.Pro281Arg
ENST00000652231.1:c.842C>G	ENSP00000498804.1:p.Pro281Arg
ENST00000326873.11:c.842C>G	ENSP00000324856.6:p.Pro281Arg
ENST00000586243.5:c.842C>G	ENSP00000467240.2:p.Pro281Arg
ENST00000586358.5:n.740C>G
ENST00000589152.5:n.932C>G
ENST00000591133.2:n.813C>G
NM_000455.4:c.842C>G , LRG_319t1:c.842C>G	NP_000446.1:p.Pro281Arg
XM_005259617.1:c.842C>G	XP_005259674.1:p.Pro281Arg
XM_005259618.3:c.842C>G	XP_005259675.1:p.Pro281Arg
XM_011528209.1:c.620C>G	XP_011526511.1:p.Pro207Arg
XR_936204.1:n.1467C>G
XM_005259617.3:c.842C>G	XP_005259674.1:p.Pro281Arg
XM_011528209.2:c.620C>G	XP_011526511.1:p.Pro207Arg
XR_001753738.2:n.1467C>G
XR_001753739.1:n.1467C>G
XR_001753740.2:n.1467C>G
NM_000455.5:c.842C>G MANE Select	NP_000446.1:p.Pro281Arg