Canonical Allele Identifier: CA1445207811
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156525_25156526delinsAG , CM000666.2:g.25156525_25156526delinsAG GRCh38
NC_000004.11:g.25158147_25158148delinsAG , CM000666.1:g.25158147_25158148delinsAG GRCh37
NC_000004.10:g.24767245_24767246delinsAG NCBI36
NG_028222.1:g.9057_9058delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.389-331_389-330delinsCT MANE Select ENSP00000371535.2:n.389-331_389-330delinsCT
ENST00000680581.1:c.389-331_389-330delinsCT ENSP00000506483.1:n.389-331_389-330delinsCT
ENST00000680824.1:n.1605-331_1605-330delinsCT
ENST00000681071.1:n.681-331_681-330delinsCT
ENST00000681166.1:n.1436-331_1436-330delinsCT
ENST00000681341.1:n.1530-331_1530-330delinsCT
ENST00000681640.1:n.483-331_483-330delinsCT
ENST00000681948.1:c.644-331_644-330delinsCT ENSP00000505991.1:n.644-331_644-330delinsCT
ENST00000358971.7:c.*187-331_*187-330delinsCT ENSP00000351857.3:n.*187-331_*187-330delinsCT
ENST00000382103.6:c.389-331_389-330delinsCT ENSP00000371535.2:n.389-331_389-330delinsCT
ENST00000514585.5:c.*90-331_*90-330delinsCT ENSP00000421880.1:n.*90-331_*90-330delinsCT
NM_016955.3:c.389-331_389-330delinsCT NP_058651.3:n.389-331_389-330delinsCT
XM_005248168.2:c.152-331_152-330delinsCT XP_005248225.1:n.152-331_152-330delinsCT
XM_006713965.2:c.209-331_209-330delinsCT XP_006714028.1:n.209-331_209-330delinsCT
XM_011513846.1:c.386-331_386-330delinsCT XP_011512148.1:n.386-331_386-330delinsCT
XM_011513847.1:c.356-331_356-330delinsCT XP_011512149.1:n.356-331_356-330delinsCT
XM_011513848.1:c.209-331_209-330delinsCT XP_011512150.1:n.209-331_209-330delinsCT
XM_011513846.2:c.386-331_386-330delinsCT XP_011512148.1:n.386-331_386-330delinsCT
XM_011513847.2:c.356-331_356-330delinsCT XP_011512149.1:n.356-331_356-330delinsCT
XM_017008277.1:c.644-331_644-330delinsCT XP_016863766.1:n.644-331_644-330delinsCT
XM_017008278.1:c.-35-331_-35-330delinsCT XP_016863767.1:n.-35-331_-35-330delinsCT
NM_016955.4:c.389-331_389-330delinsCT MANE Select NP_058651.3:n.389-331_389-330delinsCT