Canonical Allele Identifier: CA1445208263
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156707_25156726delinsCAAAAAAAAAAAAAAAAAAA , CM000666.2:g.25156707_25156726delinsCAAAAAAAAAAAAAAAAAAA GRCh38
NC_000004.11:g.25158329_25158348delinsCAAAAAAAAAAAAAAAAAAA , CM000666.1:g.25158329_25158348delinsCAAAAAAAAAAAAAAAAAAA GRCh37
NC_000004.10:g.24767427_24767446delinsCAAAAAAAAAAAAAAAAAAA NCBI36
NG_028222.1:g.8857_8876delinsTTTTTTTTTTTTTTTTTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.388+130_388+149delinsTTTTTTTTTTTTTTTTTTTG MANE Select ENSP00000371535.2:n.388+130_388+149delinsTTTTTTTTTTTTTTTTTTTG...
ENST00000680581.1:c.388+130_388+149delinsTTTTTTTTTTTTTTTTTTTG ENSP00000506483.1:n.388+130_388+149delinsTTTTTTTTTTTTTTTTTTTG...
ENST00000680824.1:n.1604+130_1604+149delinsTTTTTTTTTTTTTTTTTTTG
ENST00000681071.1:n.680+130_680+149delinsTTTTTTTTTTTTTTTTTTTG
ENST00000681166.1:n.1435+130_1435+149delinsTTTTTTTTTTTTTTTTTTTG
ENST00000681341.1:n.1529+130_1529+149delinsTTTTTTTTTTTTTTTTTTTG
ENST00000681640.1:n.482+130_482+149delinsTTTTTTTTTTTTTTTTTTTG
ENST00000681948.1:c.643+130_643+149delinsTTTTTTTTTTTTTTTTTTTG ENSP00000505991.1:n.643+130_643+149delinsTTTTTTTTTTTTTTTTTTTG...
ENST00000358971.7:c.*186+130_*186+149delinsTTTTTTTTTTTTTTTTTTTG ENSP00000351857.3:n.*186+130_*186+149delinsTTTTTTTTTTTTTTTTTT...
ENST00000382103.6:c.388+130_388+149delinsTTTTTTTTTTTTTTTTTTTG ENSP00000371535.2:n.388+130_388+149delinsTTTTTTTTTTTTTTTTTTTG...
ENST00000514585.5:c.*89+130_*89+149delinsTTTTTTTTTTTTTTTTTTTG ENSP00000421880.1:n.*89+130_*89+149delinsTTTTTTTTTTTTTTTTTTTG...
NM_016955.3:c.388+130_388+149delinsTTTTTTTTTTTTTTTTTTTG NP_058651.3:n.388+130_388+149delinsTTTTTTTTTTTTTTTTTTTG
XM_005248168.2:c.151+130_151+149delinsTTTTTTTTTTTTTTTTTTTG XP_005248225.1:n.151+130_151+149delinsTTTTTTTTTTTTTTTTTTTG
XM_006713965.2:c.208+130_208+149delinsTTTTTTTTTTTTTTTTTTTG XP_006714028.1:n.208+130_208+149delinsTTTTTTTTTTTTTTTTTTTG
XM_011513846.1:c.385+130_385+149delinsTTTTTTTTTTTTTTTTTTTG XP_011512148.1:n.385+130_385+149delinsTTTTTTTTTTTTTTTTTTTG
XM_011513847.1:c.355+130_355+149delinsTTTTTTTTTTTTTTTTTTTG XP_011512149.1:n.355+130_355+149delinsTTTTTTTTTTTTTTTTTTTG
XM_011513848.1:c.208+130_208+149delinsTTTTTTTTTTTTTTTTTTTG XP_011512150.1:n.208+130_208+149delinsTTTTTTTTTTTTTTTTTTTG
XM_011513846.2:c.385+130_385+149delinsTTTTTTTTTTTTTTTTTTTG XP_011512148.1:n.385+130_385+149delinsTTTTTTTTTTTTTTTTTTTG
XM_011513847.2:c.355+130_355+149delinsTTTTTTTTTTTTTTTTTTTG XP_011512149.1:n.355+130_355+149delinsTTTTTTTTTTTTTTTTTTTG
XM_017008277.1:c.643+130_643+149delinsTTTTTTTTTTTTTTTTTTTG XP_016863766.1:n.643+130_643+149delinsTTTTTTTTTTTTTTTTTTTG
XM_017008278.1:c.-36+130_-36+149delinsTTTTTTTTTTTTTTTTTTTG XP_016863767.1:n.-36+130_-36+149delinsTTTTTTTTTTTTTTTTTTTG
NM_016955.4:c.388+130_388+149delinsTTTTTTTTTTTTTTTTTTTG MANE Select NP_058651.3:n.388+130_388+149delinsTTTTTTTTTTTTTTTTTTTG