Canonical Allele Identifier: CA2582342344

Gene: STK11

Linked Data

• ClinVar Variation Id: 2586601
• ClinVar RCV Id: RCV003358372

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220560_1220581dup , CM000681.2:g.1220560_1220581dup	GRCh38
NC_000019.9:g.1220559_1220580dup , CM000681.1:g.1220559_1220580dup	GRCh37
NC_000019.8:g.1171559_1171580dup	NCBI36
NG_007460.2:g.36154_36175dup , LRG_319:g.36154_36175dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.598-21_598dup
ENST00000585748.3:c.226-21_226dup
ENST00000585851.2:c.424-21_424dup
ENST00000326873.12:c.598-21_598dup
ENST00000652231.1:c.598-21_598dup
ENST00000326873.11:c.598-21_598dup
ENST00000585851.1:c.424-21_424dup
ENST00000586243.5:c.598-21_598dup
ENST00000586358.5:n.475_496dup
ENST00000589152.5:n.688-21_688dup
ENST00000591133.2:n.548_569dup
NM_000455.4:c.598-21_598dup , LRG_319t1:c.598-21_598dup
XM_005259617.1:c.598-21_598dup
XM_005259618.3:c.598-21_598dup
XM_011528209.1:c.376-21_376dup
XR_936204.1:n.1223-21_1223dup
XM_005259617.3:c.598-21_598dup
XM_011528209.2:c.376-21_376dup
XR_001753738.2:n.1223-21_1223dup
XR_001753739.1:n.1223-21_1223dup
XR_001753740.2:n.1223-21_1223dup
NM_000455.5:c.598-21_598dup