Canonical Allele Identifier: CA2317593710
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226532_1226559delinsAGGCGGCGCAGCTGAGCACCAAATCCAG , CM000681.2:g.1226532_1226559delinsAGGCGGCGCAGCTGAGCACCAAATCCAG GRCh38
NC_000019.9:g.1226531_1226558delinsAGGCGGCGCAGCTGAGCACCAAATCCAG , CM000681.1:g.1226531_1226558delinsAGGCGGCGCAGCTGAGCACCAAATCCAG GRCh37
NC_000019.8:g.1177531_1177558delinsAGGCGGCGCAGCTGAGCACCAAATCCAG NCBI36
NG_007460.2:g.42126_42153delinsAGGCGGCGCAGCTGAGCACCAAATCCAG , LRG_319:g.42126_42153delinsAGGCGGCGCAGCTGAGCACCAAATCCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.*2788_*2815delinsAGGCGGCGCAGCTGAGCACCAAATCCAG ENSP00000490268.2:n.*2788_*2815delinsAGGC...
ENST00000585748.3:c.815_842delinsAGGCGGCGCAGCTGAGCACCAAATCCAG ENSP00000477641.2:p.Glu272=
ENST00000585851.2:c.1013_1040delinsAGGCGGCGCAGCTGAGCACCAAATCCAG ENSP00000467912.2:p.Glu338=
ENST00000326873.12:c.1187_1214delinsAGGCGGCGCAGCTGAGCACCAAATCCAG MANE Select ENSP00000324856.6:p.Glu396=
ENST00000326873.11:c.1187_1214delinsAGGCGGCGCAGCTGAGCACCAAATCCAG ENSP00000324856.6:p.Glu396=
ENST00000585465.2:n.2920_2947delinsAGGCGGCGCAGCTGAGCACCAAATCCAG
ENST00000586243.5:c.1187_1214delinsAGGCGGCGCAGCTGAGCACCAAATCCAG ENSP00000467240.2:p.Glu396=
ENST00000589152.5:n.1885_1912delinsAGGCGGCGCAGCTGAGCACCAAATCCAG
NM_000455.4:c.1187_1214delinsAGGCGGCGCAGCTGAGCACCAAATCCAG , LRG_319t1:c.1187_1214delinsAGGCGGCGCAGCTGAGCACCAAATCCAG NP_000446.1:p.Glu396=
XM_005259617.1:c.1182_1209delinsAGGCGGCGCAGCTGAGCACCAAATCCAG XP_005259674.1:p.Arg394=
XM_011528209.1:c.960_987delinsAGGCGGCGCAGCTGAGCACCAAATCCAG XP_011526511.1:p.Arg320=
XM_005259617.3:c.1182_1209delinsAGGCGGCGCAGCTGAGCACCAAATCCAG XP_005259674.1:p.Arg394=
XM_011528209.2:c.960_987delinsAGGCGGCGCAGCTGAGCACCAAATCCAG XP_011526511.1:p.Arg320=
XR_001753738.2:n.1993_2020delinsAGGCGGCGCAGCTGAGCACCAAATCCAG
XR_001753740.2:n.1963_1990delinsAGGCGGCGCAGCTGAGCACCAAATCCAG
NM_000455.5:c.1187_1214delinsAGGCGGCGCAGCTGAGCACCAAATCCAG MANE Select NP_000446.1:p.Glu396=