Canonical Allele Identifier: CA916081945

Gene: STK11

Linked Data

• ClinVar Variation Id: 852377
• ClinVar RCV Id: RCV001056972

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220654_1222339del , CM000681.2:g.1220654_1222339del	GRCh38
NC_000019.9:g.1220653_1222338del , CM000681.1:g.1220653_1222338del	GRCh37
NC_000019.8:g.1171653_1173338del	NCBI36
NG_007460.2:g.36248_37933del , LRG_319:g.36248_37933del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.671_920+333del
ENST00000585748.3:c.299_548+333del
ENST00000585851.2:c.497_746+333del
ENST00000326873.12:c.671_920+333del
ENST00000652231.1:c.671_920+333del
ENST00000326873.11:c.671_920+333del
ENST00000586243.5:c.671_920+333del
ENST00000589152.5:n.761_1618+333del
ENST00000591133.2:n.642_891+333del
NM_000455.4:c.671_920+333del , LRG_319t1:c.671_920+333del
XM_005259617.1:c.671_920+333del
XM_005259618.3:c.671_920+333del
XM_011528209.1:c.449_698+333del
XR_936204.1:n.1296_1696+333del
XM_005259617.3:c.671_920+333del
XM_011528209.2:c.449_698+333del
XR_001753738.2:n.1296_1726+333del
XR_001753739.1:n.1296_1726+333del
XR_001753740.2:n.1296_1696+333del
NM_000455.5:c.671_920+333del