Canonical Allele Identifier: CA2695227925
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1222985_1223172del , CM000681.2:g.1222985_1223172del GRCh38
NC_000019.9:g.1222984_1223171del , CM000681.1:g.1222984_1223171del GRCh37
NC_000019.8:g.1173984_1174171del NCBI36
NG_007460.2:g.38579_38766del , LRG_319:g.38579_38766del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.921_1108del
ENST00000585748.3:c.549_736del
ENST00000585851.2:c.747_934del
ENST00000326873.12:c.921_1108del
ENST00000652231.1:c.921_1108del
ENST00000326873.11:c.921_1108del
ENST00000586243.5:c.921_1108del
ENST00000589152.5:n.1619_1806del
NM_000455.4:c.921_1108del , LRG_319t1:c.921_1108del
XM_005259617.1:c.921_1108del
XM_005259618.3:c.921_1108del
XM_011528209.1:c.699_886del
XR_936204.1:n.1697_1884del
XM_005259617.3:c.921_1108del
XM_011528209.2:c.699_886del
XR_001753738.2:n.1727_1914del
XR_001753739.1:n.1727_1914del
XR_001753740.2:n.1697_1884del
NM_000455.5:c.921_1108del