Canonical Allele Identifier: CA2317593799
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226629_1226655delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC , CM000681.2:g.1226629_1226655delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC GRCh38
NC_000019.9:g.1226628_1226654delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC , CM000681.1:g.1226628_1226654delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC GRCh37
NC_000019.8:g.1177628_1177654delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC NCBI36
NG_007460.2:g.42223_42249delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC , LRG_319:g.42223_42249delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2885_*2911delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC ENSP00000490268.2:n.*2885_*2911delinsGGCCTGCAAGCAGCAGTGAGGCTG...
ENST00000585748.3:c.912_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC ENSP00000477641.2:n.[c.912_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGC...
ENST00000585851.2:c.1110_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC ENSP00000467912.2:n.[c.1110_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGG...
ENST00000326873.12:c.1284_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC MANE Select ENSP00000324856.6:n.[c.1284_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGG...
ENST00000326873.11:c.1284_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC ENSP00000324856.6:n.[c.1284_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGG...
ENST00000585465.2:n.3017_3043delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC
ENST00000586243.5:c.1281_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC ENSP00000467240.2:n.[c.1281_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGG...
ENST00000589152.5:n.1982_2008delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC
NM_000455.4:c.1284_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC , LRG_319t1:c.1284_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC NP_000446.1:n.[c.1284_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC;Ser...
XM_005259617.1:c.1279_1305delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC XP_005259674.1:p.Gly427=
XM_011528209.1:c.1057_1083delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC XP_011526511.1:p.Gly353=
XM_005259617.3:c.1279_1305delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC XP_005259674.1:p.Gly427=
XM_011528209.2:c.1057_1083delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC XP_011526511.1:p.Gly353=
XR_001753738.2:n.2090_2116delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC
XR_001753740.2:n.2060_2086delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC
NM_000455.5:c.1284_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC MANE Select NP_000446.1:n.[c.1284_*8delinsGGCCTGCAAGCAGCAGTGAGGCTGGCC;Ser...