Canonical Allele Identifier: CA2695227923
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1222983_1222985del , CM000681.2:g.1222983_1222985del GRCh38
NC_000019.9:g.1222982_1222984del , CM000681.1:g.1222982_1222984del GRCh37
NC_000019.8:g.1173982_1173984del NCBI36
NG_007460.2:g.38577_38579del , LRG_319:g.38577_38579del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.921-2_921del
ENST00000585748.3:c.549-2_549del
ENST00000585851.2:c.747-2_747del
ENST00000326873.12:c.921-2_921del
ENST00000652231.1:c.921-2_921del
ENST00000326873.11:c.921-2_921del
ENST00000586243.5:c.921-2_921del
ENST00000589152.5:n.1619-2_1619del
ENST00000591133.2:n.892-2_892del
NM_000455.4:c.921-2_921del , LRG_319t1:c.921-2_921del
XM_005259617.1:c.921-2_921del
XM_005259618.3:c.921-2_921del
XM_011528209.1:c.699-2_699del
XR_936204.1:n.1697-2_1697del
XM_005259617.3:c.921-2_921del
XM_011528209.2:c.699-2_699del
XR_001753738.2:n.1727-2_1727del
XR_001753739.1:n.1727-2_1727del
XR_001753740.2:n.1697-2_1697del
NM_000455.5:c.921-2_921del