Canonical Allele Identifier: CA402951344
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428755
ClinVar RCV Id: RCV000492545 RCV000709574
dbSNP Id: rs1131690920
gnomAD v4: 19-1222007-G-A
MyVariant Identifiers: chr19:g.1222006G>A (hg19) chr19:g.1222007G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1222007G>A , CM000681.2:g.1222007G>A GRCh38
NC_000019.9:g.1222006G>A , CM000681.1:g.1222006G>A GRCh37
NC_000019.8:g.1173006G>A NCBI36
NG_007460.2:g.37601G>A , LRG_319:g.37601G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.920+1G>A ENSP00000490268.2:n.920+1G>A
ENST00000585748.3:c.548+1G>A ENSP00000477641.2:n.548+1G>A
ENST00000585851.2:c.746+1G>A ENSP00000467912.2:n.746+1G>A
ENST00000326873.12:c.920+1G>A MANE Select ENSP00000324856.6:n.920+1G>A
ENST00000652231.1:c.920+1G>A ENSP00000498804.1:n.920+1G>A
ENST00000326873.11:c.920+1G>A ENSP00000324856.6:n.920+1G>A
ENST00000586243.5:c.920+1G>A ENSP00000467240.2:n.920+1G>A
ENST00000589152.5:n.1618+1G>A
ENST00000591133.2:n.891+1G>A
NM_000455.4:c.920+1G>A , LRG_319t1:c.920+1G>A NP_000446.1:n.920+1G>A
XM_005259617.1:c.920+1G>A XP_005259674.1:n.920+1G>A
XM_005259618.3:c.920+1G>A XP_005259675.1:n.920+1G>A
XM_011528209.1:c.698+1G>A XP_011526511.1:n.698+1G>A
XR_936204.1:n.1696+1G>A
XM_005259617.3:c.920+1G>A XP_005259674.1:n.920+1G>A
XM_011528209.2:c.698+1G>A XP_011526511.1:n.698+1G>A
XR_001753738.2:n.1726+1G>A
XR_001753739.1:n.1726+1G>A
XR_001753740.2:n.1696+1G>A
NM_000455.5:c.920+1G>A MANE Select NP_000446.1:n.920+1G>A
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