Canonical Allele Identifier: CA2317593429

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226121_1226156delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT , CM000681.2:g.1226121_1226156delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	GRCh38
NC_000019.9:g.1226120_1226155delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT , CM000681.1:g.1226120_1226155delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	GRCh37
NC_000019.8:g.1177120_1177155delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	NCBI36
NG_007460.2:g.41715_41750delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT , LRG_319:g.41715_41750delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2377_*2412delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	ENSP00000490268.2:n.*2377_*2412delinsGGAGGGTCCTGCCTTGTCAGCTTG...
ENST00000585748.3:c.737-333_737-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	ENSP00000477641.2:n.737-333_737-298delinsGGAGGGTCCTGCCTTGTCAG...
ENST00000585851.2:c.935-333_935-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	ENSP00000467912.2:n.935-333_935-298delinsGGAGGGTCCTGCCTTGTCAG...
ENST00000326873.12:c.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT MANE Select	ENSP00000324856.6:n.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTC...
ENST00000326873.11:c.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	ENSP00000324856.6:n.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTC...
ENST00000585465.2:n.2509_2544delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT
ENST00000586243.5:c.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	ENSP00000467240.2:n.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTC...
ENST00000589152.5:n.1807-333_1807-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT
NM_000455.4:c.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT , LRG_319t1:c.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	NP_000446.1:n.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTCAGCTTG...
XM_005259617.1:c.1109-338_1109-303delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	XP_005259674.1:n.1109-338_1109-303delinsGGAGGGTCCTGCCTTGTCAGC...
XM_011528209.1:c.887-338_887-303delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	XP_011526511.1:n.887-338_887-303delinsGGAGGGTCCTGCCTTGTCAGCTT...
XM_005259617.3:c.1109-338_1109-303delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	XP_005259674.1:n.1109-338_1109-303delinsGGAGGGTCCTGCCTTGTCAGC...
XM_011528209.2:c.887-338_887-303delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT	XP_011526511.1:n.887-338_887-303delinsGGAGGGTCCTGCCTTGTCAGCTT...
XR_001753738.2:n.1915-333_1915-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT
XR_001753740.2:n.1885-333_1885-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT
NM_000455.5:c.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTCAGCTTGCCTCCTACTCGT MANE Select	NP_000446.1:n.1109-333_1109-298delinsGGAGGGTCCTGCCTTGTCAGCTTG...