Canonical Allele Identifier: CA2580096055

Gene: STK11

Linked Data

• ClinVar Variation Id: 1742191
• ClinVar RCV Id: RCV002330459

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220352_1220373del , CM000681.2:g.1220352_1220373del	GRCh38
NC_000019.9:g.1220351_1220372del , CM000681.1:g.1220351_1220372del	GRCh37
NC_000019.8:g.1171351_1171372del	NCBI36
NG_007460.2:g.35946_35967del , LRG_319:g.35946_35967del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.465-21_465del
ENST00000585748.3:c.93-21_93del
ENST00000585851.2:c.291-21_291del
ENST00000326873.12:c.465-21_465del
ENST00000652231.1:c.465-21_465del
ENST00000326873.11:c.465-21_465del
ENST00000585851.1:c.291-21_291del
ENST00000586243.5:c.465-21_465del
ENST00000586358.5:n.288-21_288del
ENST00000589152.5:n.555-21_555del
ENST00000591133.2:n.340_361del
NM_000455.4:c.465-21_465del , LRG_319t1:c.465-21_465del
XM_005259617.1:c.465-21_465del
XM_005259618.3:c.465-21_465del
XM_011528209.1:c.243-21_243del
XR_936204.1:n.1090-21_1090del
XM_005259617.3:c.465-21_465del
XM_011528209.2:c.243-21_243del
XR_001753738.2:n.1090-21_1090del
XR_001753739.1:n.1090-21_1090del
XR_001753740.2:n.1090-21_1090del
NM_000455.5:c.465-21_465del