Canonical Allele Identifier: CA2580096141

Gene: STK11

Linked Data

• ClinVar Variation Id: 2028252
• ClinVar RCV Id: RCV002876047

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223097_1223181dup , CM000681.2:g.1223097_1223181dup	GRCh38
NC_000019.9:g.1223096_1223180dup , CM000681.1:g.1223096_1223180dup	GRCh37
NC_000019.8:g.1174096_1174180dup	NCBI36
NG_007460.2:g.38691_38775dup , LRG_319:g.38691_38775dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1033_1108+9dup
ENST00000585748.3:c.661_736+9dup
ENST00000585851.2:c.859_934+9dup
ENST00000326873.12:c.1033_1108+9dup
ENST00000652231.1:c.1033_1108+9dup
ENST00000326873.11:c.1033_1108+9dup
ENST00000586243.5:c.1033_1108+9dup
ENST00000589152.5:n.1731_1806+9dup
NM_000455.4:c.1033_1108+9dup , LRG_319t1:c.1033_1108+9dup
XM_005259617.1:c.1033_1108+9dup
XM_005259618.3:c.1033_1108+9dup
XM_011528209.1:c.811_886+9dup
XR_936204.1:n.1809_1884+9dup
XM_005259617.3:c.1033_1108+9dup
XM_011528209.2:c.811_886+9dup
XR_001753738.2:n.1839_1914+9dup
XR_001753739.1:n.1839_1914+9dup
XR_001753740.2:n.1809_1884+9dup
NM_000455.5:c.1033_1108+9dup