Canonical Allele Identifier: CA023036

Gene: STK11

Linked Data

• ClinVar Variation Id: 142034
• ClinVar RCV Id: RCV000130832 ; RCV000199796 ; RCV001355110 ; RCV001705929 ; RCV003321514 ; RCV003492604
• dbSNP Id: rs567202367
• ExAC: 19:1220367 C / T
• gnomAD v2: 19-1220367-C-T
• gnomAD v3: 19-1220368-C-T
• gnomAD v4: 19-1220368-C-T
• MyVariant Identifiers: chr19:g.1220367C>T (hg19) ; chr19:g.1220368C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220368C>T , CM000681.2:g.1220368C>T	GRCh38
NC_000019.9:g.1220367C>T , CM000681.1:g.1220367C>T	GRCh37
NC_000019.8:g.1171367C>T	NCBI36
NG_007460.2:g.35962C>T , LRG_319:g.35962C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.465-5C>T	ENSP00000490268.2:n.465-5C>T
ENST00000585748.3:c.93-5C>T	ENSP00000477641.2:n.93-5C>T
ENST00000585851.2:c.291-5C>T	ENSP00000467912.2:n.291-5C>T
ENST00000326873.12:c.465-5C>T MANE Select	ENSP00000324856.6:n.465-5C>T
ENST00000652231.1:c.465-5C>T	ENSP00000498804.1:n.465-5C>T
ENST00000326873.11:c.465-5C>T	ENSP00000324856.6:n.465-5C>T
ENST00000585851.1:c.291-5C>T	ENSP00000467912.1:n.291-5C>T
ENST00000586243.5:c.465-5C>T	ENSP00000467240.2:n.465-5C>T
ENST00000586358.5:n.288-5C>T
ENST00000589152.5:n.555-5C>T
ENST00000591133.2:n.356C>T
NM_000455.4:c.465-5C>T , LRG_319t1:c.465-5C>T	NP_000446.1:n.465-5C>T
XM_005259617.1:c.465-5C>T	XP_005259674.1:n.465-5C>T
XM_005259618.3:c.465-5C>T	XP_005259675.1:n.465-5C>T
XM_011528209.1:c.243-5C>T	XP_011526511.1:n.243-5C>T
XR_936204.1:n.1090-5C>T
XM_005259617.3:c.465-5C>T	XP_005259674.1:n.465-5C>T
XM_011528209.2:c.243-5C>T	XP_011526511.1:n.243-5C>T
XR_001753738.2:n.1090-5C>T
XR_001753739.1:n.1090-5C>T
XR_001753740.2:n.1090-5C>T
NM_000455.5:c.465-5C>T MANE Select	NP_000446.1:n.465-5C>T