Canonical Allele Identifier: CA916081940

Gene: STK11

Linked Data

• ClinVar Variation Id: 845797
• ClinVar RCV Id: RCV001048932

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218407_1222986del , CM000681.2:g.1218407_1222986del	GRCh38
NC_000019.9:g.1218406_1222985del , CM000681.1:g.1218406_1222985del	GRCh37
NC_000019.8:g.1169406_1173985del	NCBI36
NG_007460.2:g.34001_38580del , LRG_319:g.34001_38580del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.291-10_922del
ENST00000585748.3:c.-82-10_550del
ENST00000585851.2:c.291-1966_748del
ENST00000326873.12:c.291-10_922del
ENST00000652231.1:c.291-10_922del
ENST00000326873.11:c.291-10_922del
ENST00000586243.5:c.291-10_922del
ENST00000589152.5:n.381-10_1620del
NM_000455.4:c.291-10_922del , LRG_319t1:c.291-10_922del
XM_005259617.1:c.291-10_922del
XM_005259618.3:c.291-10_922del
XM_011528209.1:c.69-10_700del
XR_936204.1:n.916-10_1698del
XM_005259617.3:c.291-10_922del
XM_011528209.2:c.69-10_700del
XR_001753738.2:n.916-10_1728del
XR_001753739.1:n.916-10_1728del
XR_001753740.2:n.916-10_1698del
NM_000455.5:c.291-10_922del