Canonical Allele Identifier: CA2695238732
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156707_25156710delinsCAAA , CM000666.2:g.25156707_25156710delinsCAAA GRCh38
NC_000004.11:g.25158329_25158332delinsCAAA , CM000666.1:g.25158329_25158332delinsCAAA GRCh37
NC_000004.10:g.24767427_24767430delinsCAAA NCBI36
NG_028222.1:g.8873_8876delinsTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.388+146_388+149delinsTTTG MANE Select ENSP00000371535.2:n.388+146_388+149delinsTTTG
ENST00000680581.1:c.388+146_388+149delinsTTTG ENSP00000506483.1:n.388+146_388+149delinsTTTG
ENST00000680824.1:n.1604+146_1604+149delinsTTTG
ENST00000681071.1:n.680+146_680+149delinsTTTG
ENST00000681166.1:n.1435+146_1435+149delinsTTTG
ENST00000681341.1:n.1529+146_1529+149delinsTTTG
ENST00000681640.1:n.482+146_482+149delinsTTTG
ENST00000681948.1:c.643+146_643+149delinsTTTG ENSP00000505991.1:n.643+146_643+149delinsTTTG
ENST00000358971.7:c.*186+146_*186+149delinsTTTG ENSP00000351857.3:n.*186+146_*186+149delinsTTTG
ENST00000382103.6:c.388+146_388+149delinsTTTG ENSP00000371535.2:n.388+146_388+149delinsTTTG
ENST00000514585.5:c.*89+146_*89+149delinsTTTG ENSP00000421880.1:n.*89+146_*89+149delinsTTTG
NM_016955.3:c.388+146_388+149delinsTTTG NP_058651.3:n.388+146_388+149delinsTTTG
XM_005248168.2:c.151+146_151+149delinsTTTG XP_005248225.1:n.151+146_151+149delinsTTTG
XM_006713965.2:c.208+146_208+149delinsTTTG XP_006714028.1:n.208+146_208+149delinsTTTG
XM_011513846.1:c.385+146_385+149delinsTTTG XP_011512148.1:n.385+146_385+149delinsTTTG
XM_011513847.1:c.355+146_355+149delinsTTTG XP_011512149.1:n.355+146_355+149delinsTTTG
XM_011513848.1:c.208+146_208+149delinsTTTG XP_011512150.1:n.208+146_208+149delinsTTTG
XM_011513846.2:c.385+146_385+149delinsTTTG XP_011512148.1:n.385+146_385+149delinsTTTG
XM_011513847.2:c.355+146_355+149delinsTTTG XP_011512149.1:n.355+146_355+149delinsTTTG
XM_017008277.1:c.643+146_643+149delinsTTTG XP_016863766.1:n.643+146_643+149delinsTTTG
XM_017008278.1:c.-36+146_-36+149delinsTTTG XP_016863767.1:n.-36+146_-36+149delinsTTTG
NM_016955.4:c.388+146_388+149delinsTTTG MANE Select NP_058651.3:n.388+146_388+149delinsTTTG