Canonical Allele Identifier: CA2760764312
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25120604_25120605insTTCAATTATTATTCAGGTTGTGAGACTTCTAAAATGACCAAATTTCTGTGTATGCAAAACTGGACTTTTTTCAGTTA , CM000666.2:g.25120604_25120605insTTCAATTATTATTCAGGTTGTGAGACTTCTAAAATGACCAAATTTCTGTGTATGCAAAACTGGACTTTTTTCAGTTA GRCh38
NC_000004.11:g.25122226_25122227insTTCAATTATTATTCAGGTTGTGAGACTTCTAAAATGACCAAATTTCTGTGTATGCAAAACTGGACTTTTTTCAGTTA , CM000666.1:g.25122226_25122227insTTCAATTATTATTCAGGTTGTGAGACTTCTAAAATGACCAAATTTCTGTGTATGCAAAACTGGACTTTTTTCAGTTA GRCh37
NC_000004.10:g.24731324_24731325insTTCAATTATTATTCAGGTTGTGAGACTTCTAAAATGACCAAATTTCTGTGTATGCAAAACTGGACTTTTTTCAGTTA NCBI36
NG_028222.1:g.45048_45049insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT MANE Select ENSP00000371535.2:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTT...
ENST00000680581.1:c.*3776_*3777insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT ENSP00000506483.1:n.*3776_*3777insAATTGAATAACTGAAAAAAGTCCAGTT...
ENST00000680824.1:n.6118_6119insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT
ENST00000681071.1:n.5194_5195insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT
ENST00000681341.1:n.5949_5950insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT
ENST00000681374.1:n.4258_4259insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT
ENST00000681948.1:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT ENSP00000505991.1:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTT...
ENST00000382103.6:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT ENSP00000371535.2:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTT...
NM_016955.3:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT NP_058651.3:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCAT...
XM_005248168.2:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT XP_005248225.1:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTG...
XM_006713965.2:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT XP_006714028.1:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTG...
XM_011513846.1:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT XP_011512148.1:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTG...
XM_011513847.1:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT XP_011512149.1:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTG...
XM_011513848.1:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT XP_011512150.1:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTG...
XM_011513846.2:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT XP_011512148.1:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTG...
XM_011513847.2:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT XP_011512149.1:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTG...
XM_017008277.1:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT XP_016863766.1:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTG...
XM_017008278.1:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT XP_016863767.1:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTG...
NM_016955.4:c.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCATACACAGAAATTTGGTCATTTTAGAAGTCTCACAACCTGAATAAT MANE Select NP_058651.3:n.*3396_*3397insAATTGAATAACTGAAAAAAGTCCAGTTTTGCAT...