Canonical Allele Identifier: CA402949192

Gene: STK11

Linked Data

• ClinVar Variation Id: 2811478
• ClinVar RCV Id: RCV003618402
• dbSNP Id: rs2145424551
• gnomAD v4: 19-1220471-G-A
• MyVariant Identifiers: chr19:g.1220470G>A (hg19) ; chr19:g.1220471G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220471G>A , CM000681.2:g.1220471G>A	GRCh38
NC_000019.9:g.1220470G>A , CM000681.1:g.1220470G>A	GRCh37
NC_000019.8:g.1171470G>A	NCBI36
NG_007460.2:g.36065G>A , LRG_319:g.36065G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.563G>A	ENSP00000490268.2:p.Gly188Asp
ENST00000585748.3:c.191G>A	ENSP00000477641.2:p.Gly64Asp
ENST00000585851.2:c.389G>A	ENSP00000467912.2:p.Gly130Asp
ENST00000326873.12:c.563G>A MANE Select	ENSP00000324856.6:p.Gly188Asp
ENST00000652231.1:c.563G>A	ENSP00000498804.1:p.Gly188Asp
ENST00000326873.11:c.563G>A	ENSP00000324856.6:p.Gly188Asp
ENST00000585851.1:c.389G>A	ENSP00000467912.1:p.Gly130Asp
ENST00000586243.5:c.563G>A	ENSP00000467240.2:p.Gly188Asp
ENST00000586358.5:n.386G>A
ENST00000589152.5:n.653G>A
ENST00000591133.2:n.459G>A
NM_000455.4:c.563G>A , LRG_319t1:c.563G>A	NP_000446.1:p.Gly188Asp
XM_005259617.1:c.563G>A	XP_005259674.1:p.Gly188Asp
XM_005259618.3:c.563G>A	XP_005259675.1:p.Gly188Asp
XM_011528209.1:c.341G>A	XP_011526511.1:p.Gly114Asp
XR_936204.1:n.1188G>A
XM_005259617.3:c.563G>A	XP_005259674.1:p.Gly188Asp
XM_011528209.2:c.341G>A	XP_011526511.1:p.Gly114Asp
XR_001753738.2:n.1188G>A
XR_001753739.1:n.1188G>A
XR_001753740.2:n.1188G>A
NM_000455.5:c.563G>A MANE Select	NP_000446.1:p.Gly188Asp