Canonical Allele Identifier: CA10642257
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 328204
dbSNP Id: rs147615524
gnomAD v2: 19-1205889-C-T
gnomAD v3: 19-1205890-C-T
gnomAD v4: 19-1205890-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1205890C>T , CM000681.2:g.1205890C>T GRCh38
NC_000019.9:g.1205889C>T , CM000681.1:g.1205889C>T GRCh37
NC_000019.8:g.1156889C>T NCBI36
NG_007460.2:g.21484C>T , LRG_319:g.21484C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.-1024C>T ENSP00000490268.2:n.-1024C>T
ENST00000585748.3:c.-82-12527C>T ENSP00000477641.2:n.-82-12527C>T
ENST00000326873.12:c.-1024C>T MANE Select ENSP00000324856.6:n.-1024C>T
ENST00000585748.2:c.-82-12527C>T ENSP00000477641.1:n.-82-12527C>T
ENST00000586243.5:c.-875C>T ENSP00000467240.2:n.-875C>T
NM_000455.4:c.-1024C>T , LRG_319t1:c.-1024C>T NP_000446.1:n.-1024C>T
NM_000455.5:c.-1024C>T MANE Select NP_000446.1:n.-1024C>T