Canonical Allele Identifier: CA023047

Gene: STK11

Linked Data

• ClinVar Variation Id: 182898
• ClinVar RCV Id: RCV000492450
• dbSNP Id: rs730881972
• MyVariant Identifiers: chr19:g.1220394G>C (hg19) ; chr19:g.1220395G>C (hg38)
• PubMed: PMID:9887330 ; PMID:15188174 ; PMID:19952941 ; PMID:26225618

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220395G>C , CM000681.2:g.1220395G>C	GRCh38
NC_000019.9:g.1220394G>C , CM000681.1:g.1220394G>C	GRCh37
NC_000019.8:g.1171394G>C	NCBI36
NG_007460.2:g.35989G>C , LRG_319:g.35989G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.487G>C	ENSP00000490268.2:p.Gly163Arg
ENST00000585748.3:c.115G>C	ENSP00000477641.2:p.Gly39Arg
ENST00000585851.2:c.313G>C	ENSP00000467912.2:p.Gly105Arg
ENST00000326873.12:c.487G>C MANE Select	ENSP00000324856.6:p.Gly163Arg
ENST00000652231.1:c.487G>C	ENSP00000498804.1:p.Gly163Arg
ENST00000326873.11:c.487G>C	ENSP00000324856.6:p.Gly163Arg
ENST00000585851.1:c.313G>C	ENSP00000467912.1:p.Gly105Arg
ENST00000586243.5:c.487G>C	ENSP00000467240.2:p.Gly163Arg
ENST00000586358.5:n.310G>C
ENST00000589152.5:n.577G>C
ENST00000591133.2:n.383G>C
NM_000455.4:c.487G>C , LRG_319t1:c.487G>C	NP_000446.1:p.Gly163Arg
XM_005259617.1:c.487G>C	XP_005259674.1:p.Gly163Arg
XM_005259618.3:c.487G>C	XP_005259675.1:p.Gly163Arg
XM_011528209.1:c.265G>C	XP_011526511.1:p.Gly89Arg
XR_936204.1:n.1112G>C
XM_005259617.3:c.487G>C	XP_005259674.1:p.Gly163Arg
XM_011528209.2:c.265G>C	XP_011526511.1:p.Gly89Arg
XR_001753738.2:n.1112G>C
XR_001753739.1:n.1112G>C
XR_001753740.2:n.1112G>C
NM_000455.5:c.487G>C MANE Select	NP_000446.1:p.Gly163Arg