Canonical Allele Identifier: CA891843672
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 576830
ClinVar RCV Id: RCV000699422

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1205800_1207204del , CM000681.2:g.1205800_1207204del GRCh38
NC_000019.9:g.1205799_1207203del , CM000681.1:g.1205799_1207203del GRCh37
NC_000019.8:g.1156799_1158203del NCBI36
NG_007460.2:g.21394_22798del , LRG_319:g.21394_22798del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.-1114_290+1del
ENST00000585748.3:c.-82-12617_-82-11213del ENSP00000477641.2:n.-82-12617_-82-11213de...
ENST00000326873.12:c.-1114_290+1del
ENST00000585748.2:c.-82-12617_-82-11213del ENSP00000477641.1:n.-82-12617_-82-11213de...
NM_000455.4:c.-1114_290+1del , LRG_319t1:c.-1114_290+1del
NM_000455.5:c.-1114_290+1del