Canonical Allele Identifier: CA10651496
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 328224
ClinVar RCV Id: RCV000386427
dbSNP Id: rs927999961
gnomAD v2: 19-1206796-C-CT
gnomAD v3: 19-1206797-C-CT
gnomAD v4: 19-1206797-C-CT
MyVariant Identifiers: chr19:g.1206806dupT (hg19) chr19:g.1206806_1206807insT (hg19) chr19:g.1206797_1206798insT (hg19) chr19:g.1206796_1206797insT (hg19) chr19:g.1206807dupT (hg38) chr19:g.1206807_1206808insT (hg38) chr19:g.1206798_1206799insT (hg38) chr19:g.1206797_1206798insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206807dup , CM000681.2:g.1206807dup GRCh38
NC_000019.9:g.1206806dup , CM000681.1:g.1206806dup GRCh37
NC_000019.8:g.1157806dup NCBI36
NG_007460.2:g.22401dup , LRG_319:g.22401dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.-107dup ENSP00000490268.2:n.-107dup
ENST00000585748.3:c.-82-11610dup ENSP00000477641.2:n.-82-11610dup
ENST00000326873.12:c.-107dup MANE Select ENSP00000324856.6:n.-107dup
ENST00000652231.1:c.-107dup ENSP00000498804.1:n.-107dup
ENST00000326873.11:c.-107dup ENSP00000324856.6:n.-107dup
ENST00000585748.2:c.-82-11610dup ENSP00000477641.1:n.-82-11610dup
ENST00000586243.5:c.-107dup ENSP00000467240.2:n.-107dup
NM_000455.4:c.-107dup , LRG_319t1:c.-107dup NP_000446.1:n.-107dup
XM_005259617.1:c.-107dup XP_005259674.1:n.-107dup
XM_005259618.3:c.-107dup XP_005259675.1:n.-107dup
XM_011528209.1:c.-460dup XP_011526511.1:n.-460dup
XR_936204.1:n.519dup
XM_005259617.3:c.-107dup XP_005259674.1:n.-107dup
XM_011528209.2:c.-460dup XP_011526511.1:n.-460dup
XR_001753738.2:n.519dup
XR_001753739.1:n.519dup
XR_001753740.2:n.519dup
NM_000455.5:c.-107dup MANE Select NP_000446.1:n.-107dup
Search 100 bp 5'
Search 100 bp 3'