Canonical Allele Identifier: CA023032

Gene: STK11

Linked Data

• ClinVar Variation Id: 127703
• ClinVar RCV Id: RCV000115599 ; RCV000144662 ; RCV000213012 ; RCV000679320 ; RCV001354249 ; RCV001798332 ; RCV001262518
• dbSNP Id: rs587780009
• ExAC: 19:1220368 G / A
• gnomAD v2: 19-1220368-G-A
• gnomAD v3: 19-1220369-G-A
• gnomAD v4: 19-1220369-G-A
• MyVariant Identifiers: chr19:g.1220368G>A (hg19) ; chr19:g.1220369G>A (hg38)
• PubMed: PMID:16287113

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220369G>A , CM000681.2:g.1220369G>A	GRCh38
NC_000019.9:g.1220368G>A , CM000681.1:g.1220368G>A	GRCh37
NC_000019.8:g.1171368G>A	NCBI36
NG_007460.2:g.35963G>A , LRG_319:g.35963G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.465-4G>A	ENSP00000490268.2:n.465-4G>A
ENST00000585748.3:c.93-4G>A	ENSP00000477641.2:n.93-4G>A
ENST00000585851.2:c.291-4G>A	ENSP00000467912.2:n.291-4G>A
ENST00000326873.12:c.465-4G>A MANE Select	ENSP00000324856.6:n.465-4G>A
ENST00000652231.1:c.465-4G>A	ENSP00000498804.1:n.465-4G>A
ENST00000326873.11:c.465-4G>A	ENSP00000324856.6:n.465-4G>A
ENST00000585851.1:c.291-4G>A	ENSP00000467912.1:n.291-4G>A
ENST00000586243.5:c.465-4G>A	ENSP00000467240.2:n.465-4G>A
ENST00000586358.5:n.288-4G>A
ENST00000589152.5:n.555-4G>A
ENST00000591133.2:n.357G>A
NM_000455.4:c.465-4G>A , LRG_319t1:c.465-4G>A	NP_000446.1:n.465-4G>A
XM_005259617.1:c.465-4G>A	XP_005259674.1:n.465-4G>A
XM_005259618.3:c.465-4G>A	XP_005259675.1:n.465-4G>A
XM_011528209.1:c.243-4G>A	XP_011526511.1:n.243-4G>A
XR_936204.1:n.1090-4G>A
XM_005259617.3:c.465-4G>A	XP_005259674.1:n.465-4G>A
XM_011528209.2:c.243-4G>A	XP_011526511.1:n.243-4G>A
XR_001753738.2:n.1090-4G>A
XR_001753739.1:n.1090-4G>A
XR_001753740.2:n.1090-4G>A
NM_000455.5:c.465-4G>A MANE Select	NP_000446.1:n.465-4G>A