Canonical Allele Identifier: CA1445208467
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156735_25156739delinsAGAAG , CM000666.2:g.25156735_25156739delinsAGAAG GRCh38
NC_000004.11:g.25158357_25158361delinsAGAAG , CM000666.1:g.25158357_25158361delinsAGAAG GRCh37
NC_000004.10:g.24767455_24767459delinsAGAAG NCBI36
NG_028222.1:g.8844_8848delinsCTTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.388+117_388+121delinsCTTCT MANE Select ENSP00000371535.2:n.388+117_388+121delinsCTTCT
ENST00000680581.1:c.388+117_388+121delinsCTTCT ENSP00000506483.1:n.388+117_388+121delinsCTTCT
ENST00000680824.1:n.1604+117_1604+121delinsCTTCT
ENST00000681071.1:n.680+117_680+121delinsCTTCT
ENST00000681166.1:n.1435+117_1435+121delinsCTTCT
ENST00000681341.1:n.1529+117_1529+121delinsCTTCT
ENST00000681640.1:n.482+117_482+121delinsCTTCT
ENST00000681948.1:c.643+117_643+121delinsCTTCT ENSP00000505991.1:n.643+117_643+121delinsCTTCT
ENST00000358971.7:c.*186+117_*186+121delinsCTTCT ENSP00000351857.3:n.*186+117_*186+121delinsCTTCT
ENST00000382103.6:c.388+117_388+121delinsCTTCT ENSP00000371535.2:n.388+117_388+121delinsCTTCT
ENST00000514585.5:c.*89+117_*89+121delinsCTTCT ENSP00000421880.1:n.*89+117_*89+121delinsCTTCT
NM_016955.3:c.388+117_388+121delinsCTTCT NP_058651.3:n.388+117_388+121delinsCTTCT
XM_005248168.2:c.151+117_151+121delinsCTTCT XP_005248225.1:n.151+117_151+121delinsCTTCT
XM_006713965.2:c.208+117_208+121delinsCTTCT XP_006714028.1:n.208+117_208+121delinsCTTCT
XM_011513846.1:c.385+117_385+121delinsCTTCT XP_011512148.1:n.385+117_385+121delinsCTTCT
XM_011513847.1:c.355+117_355+121delinsCTTCT XP_011512149.1:n.355+117_355+121delinsCTTCT
XM_011513848.1:c.208+117_208+121delinsCTTCT XP_011512150.1:n.208+117_208+121delinsCTTCT
XM_011513846.2:c.385+117_385+121delinsCTTCT XP_011512148.1:n.385+117_385+121delinsCTTCT
XM_011513847.2:c.355+117_355+121delinsCTTCT XP_011512149.1:n.355+117_355+121delinsCTTCT
XM_017008277.1:c.643+117_643+121delinsCTTCT XP_016863766.1:n.643+117_643+121delinsCTTCT
XM_017008278.1:c.-36+117_-36+121delinsCTTCT XP_016863767.1:n.-36+117_-36+121delinsCTTCT
NM_016955.4:c.388+117_388+121delinsCTTCT MANE Select NP_058651.3:n.388+117_388+121delinsCTTCT