Canonical Allele Identifier: CA402951589

Gene: STK11

Linked Data

• ClinVar Variation Id: 1498658
• ClinVar RCV Id: RCV001999321 ; RCV004045931
• dbSNP Id: rs587781643
• gnomAD v2: 19-1223037-G-C
• gnomAD v4: 19-1223038-G-C
• MyVariant Identifiers: chr19:g.1223037G>C (hg19) ; chr19:g.1223038G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223038G>C , CM000681.2:g.1223038G>C	GRCh38
NC_000019.9:g.1223037G>C , CM000681.1:g.1223037G>C	GRCh37
NC_000019.8:g.1174037G>C	NCBI36
NG_007460.2:g.38632G>C , LRG_319:g.38632G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.974G>C	ENSP00000490268.2:p.Ser325Thr
ENST00000585748.3:c.602G>C	ENSP00000477641.2:p.Ser201Thr
ENST00000585851.2:c.800G>C	ENSP00000467912.2:p.Ser267Thr
ENST00000326873.12:c.974G>C MANE Select	ENSP00000324856.6:p.Ser325Thr
ENST00000652231.1:c.974G>C	ENSP00000498804.1:p.Ser325Thr
ENST00000326873.11:c.974G>C	ENSP00000324856.6:p.Ser325Thr
ENST00000586243.5:c.974G>C	ENSP00000467240.2:p.Ser325Thr
ENST00000589152.5:n.1672G>C
ENST00000591133.2:n.945G>C
NM_000455.4:c.974G>C , LRG_319t1:c.974G>C	NP_000446.1:p.Ser325Thr
XM_005259617.1:c.974G>C	XP_005259674.1:p.Ser325Thr
XM_005259618.3:c.974G>C	XP_005259675.1:p.Ser325Thr
XM_011528209.1:c.752G>C	XP_011526511.1:p.Ser251Thr
XR_936204.1:n.1750G>C
XM_005259617.3:c.974G>C	XP_005259674.1:p.Ser325Thr
XM_011528209.2:c.752G>C	XP_011526511.1:p.Ser251Thr
XR_001753738.2:n.1780G>C
XR_001753739.1:n.1780G>C
XR_001753740.2:n.1750G>C
NM_000455.5:c.974G>C MANE Select	NP_000446.1:p.Ser325Thr