Canonical Allele Identifier: CA2695227922
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1222980_1223016del , CM000681.2:g.1222980_1223016del GRCh38
NC_000019.9:g.1222979_1223015del , CM000681.1:g.1222979_1223015del GRCh37
NC_000019.8:g.1173979_1174015del NCBI36
NG_007460.2:g.38574_38610del , LRG_319:g.38574_38610del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.921-5_952del
ENST00000585748.3:c.549-5_580del
ENST00000585851.2:c.747-5_778del
ENST00000326873.12:c.921-5_952del
ENST00000652231.1:c.921-5_952del
ENST00000326873.11:c.921-5_952del
ENST00000586243.5:c.921-5_952del
ENST00000589152.5:n.1619-5_1650del
ENST00000591133.2:n.892-5_923del
NM_000455.4:c.921-5_952del , LRG_319t1:c.921-5_952del
XM_005259617.1:c.921-5_952del
XM_005259618.3:c.921-5_952del
XM_011528209.1:c.699-5_730del
XR_936204.1:n.1697-5_1728del
XM_005259617.3:c.921-5_952del
XM_011528209.2:c.699-5_730del
XR_001753738.2:n.1727-5_1758del
XR_001753739.1:n.1727-5_1758del
XR_001753740.2:n.1697-5_1728del
NM_000455.5:c.921-5_952del