Canonical Allele Identifier: CA402951837

Gene: STK11

Linked Data

• ClinVar Variation Id: 1685153
• ClinVar RCV Id: RCV002248880 ; RCV003617950
• dbSNP Id: rs2145431252
• MyVariant Identifiers: chr19:g.1223118A>T (hg19) ; chr19:g.1223119A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223119A>T , CM000681.2:g.1223119A>T	GRCh38
NC_000019.9:g.1223118A>T , CM000681.1:g.1223118A>T	GRCh37
NC_000019.8:g.1174118A>T	NCBI36
NG_007460.2:g.38713A>T , LRG_319:g.38713A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1055A>T	ENSP00000490268.2:p.Asp352Val
ENST00000585748.3:c.683A>T	ENSP00000477641.2:p.Asp228Val
ENST00000585851.2:c.881A>T	ENSP00000467912.2:p.Asp294Val
ENST00000326873.12:c.1055A>T MANE Select	ENSP00000324856.6:p.Asp352Val
ENST00000652231.1:c.1055A>T	ENSP00000498804.1:p.Asp352Val
ENST00000326873.11:c.1055A>T	ENSP00000324856.6:p.Asp352Val
ENST00000586243.5:c.1055A>T	ENSP00000467240.2:p.Asp352Val
ENST00000589152.5:n.1753A>T
NM_000455.4:c.1055A>T , LRG_319t1:c.1055A>T	NP_000446.1:p.Asp352Val
XM_005259617.1:c.1055A>T	XP_005259674.1:p.Asp352Val
XM_005259618.3:c.1055A>T	XP_005259675.1:p.Asp352Val
XM_011528209.1:c.833A>T	XP_011526511.1:p.Asp278Val
XR_936204.1:n.1831A>T
XM_005259617.3:c.1055A>T	XP_005259674.1:p.Asp352Val
XM_011528209.2:c.833A>T	XP_011526511.1:p.Asp278Val
XR_001753738.2:n.1861A>T
XR_001753739.1:n.1861A>T
XR_001753740.2:n.1831A>T
NM_000455.5:c.1055A>T MANE Select	NP_000446.1:p.Asp352Val