Canonical Allele Identifier: CA1445207846
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156532_25156533delinsCG , CM000666.2:g.25156532_25156533delinsCG GRCh38
NC_000004.11:g.25158154_25158155delinsCG , CM000666.1:g.25158154_25158155delinsCG GRCh37
NC_000004.10:g.24767252_24767253delinsCG NCBI36
NG_028222.1:g.9050_9051delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.388+323_388+324delinsCG MANE Select ENSP00000371535.2:n.388+323_388+324delinsCG
ENST00000680581.1:c.388+323_388+324delinsCG ENSP00000506483.1:n.388+323_388+324delinsCG
ENST00000680824.1:n.1604+323_1604+324delinsCG
ENST00000681071.1:n.680+323_680+324delinsCG
ENST00000681166.1:n.1435+323_1435+324delinsCG
ENST00000681341.1:n.1529+323_1529+324delinsCG
ENST00000681640.1:n.482+323_482+324delinsCG
ENST00000681948.1:c.643+323_643+324delinsCG ENSP00000505991.1:n.643+323_643+324delinsCG
ENST00000358971.7:c.*186+323_*186+324delinsCG ENSP00000351857.3:n.*186+323_*186+324delinsCG
ENST00000382103.6:c.388+323_388+324delinsCG ENSP00000371535.2:n.388+323_388+324delinsCG
ENST00000514585.5:c.*89+323_*89+324delinsCG ENSP00000421880.1:n.*89+323_*89+324delinsCG
NM_016955.3:c.388+323_388+324delinsCG NP_058651.3:n.388+323_388+324delinsCG
XM_005248168.2:c.151+323_151+324delinsCG XP_005248225.1:n.151+323_151+324delinsCG
XM_006713965.2:c.208+323_208+324delinsCG XP_006714028.1:n.208+323_208+324delinsCG
XM_011513846.1:c.385+323_385+324delinsCG XP_011512148.1:n.385+323_385+324delinsCG
XM_011513847.1:c.355+323_355+324delinsCG XP_011512149.1:n.355+323_355+324delinsCG
XM_011513848.1:c.208+323_208+324delinsCG XP_011512150.1:n.208+323_208+324delinsCG
XM_011513846.2:c.385+323_385+324delinsCG XP_011512148.1:n.385+323_385+324delinsCG
XM_011513847.2:c.355+323_355+324delinsCG XP_011512149.1:n.355+323_355+324delinsCG
XM_017008277.1:c.643+323_643+324delinsCG XP_016863766.1:n.643+323_643+324delinsCG
XM_017008278.1:c.-36+323_-36+324delinsCG XP_016863767.1:n.-36+323_-36+324delinsCG
NM_016955.4:c.388+323_388+324delinsCG MANE Select NP_058651.3:n.388+323_388+324delinsCG