Canonical Allele Identifier: CA2670197278

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156949del , CM000666.2:g.25156949del	GRCh38
NC_000004.11:g.25158571del , CM000666.1:g.25158571del	GRCh37
NC_000004.10:g.24767669del	NCBI36
NG_028222.1:g.8635del

Transcript Alleles

HGVS	Amino-acid Change
NM_016955.4:c.296del MANE Select	NP_058651.3:p.Gly99ValfsTer16
ENST00000382103.7:c.296del MANE Select	ENSP00000371535.2:p.Gly99ValfsTer16
NM_016955.3:c.296del	NP_058651.3:p.Gly99ValfsTer16
ENST00000358971.7:c.*94del	ENSP00000351857.3:n.*94del
ENST00000382103.6:c.296del	ENSP00000371535.2:p.Gly99ValfsTer16
ENST00000514585.5:c.141del	ENSP00000421880.1:p.Ter48AspextTer?
ENST00000680581.1:c.296del	ENSP00000506483.1:p.Gly99ValfsTer16
ENST00000680824.1:n.1512del
ENST00000681071.1:n.588del
ENST00000681166.1:n.1343del
ENST00000681341.1:n.1437del
ENST00000681640.1:n.390del
ENST00000681948.1:c.551del	ENSP00000505991.1:p.Gly184ValfsTer16
XM_005248168.2:c.59del	XP_005248225.1:p.Gly20ValfsTer16
XM_006713965.2:c.116del	XP_006714028.1:p.Gly39ValfsTer16
XM_011513846.1:c.293del	XP_011512148.1:p.Gly98ValfsTer16
XM_011513846.2:c.293del	XP_011512148.1:p.Gly98ValfsTer16
XM_011513847.1:c.263del	XP_011512149.1:p.Gly88ValfsTer16
XM_011513847.2:c.263del	XP_011512149.1:p.Gly88ValfsTer16
XM_011513848.1:c.116del	XP_011512150.1:p.Gly39ValfsTer16
XM_017008277.1:c.551del	XP_016863766.1:p.Gly184ValfsTer16
XM_017008278.1:c.-128del	XP_016863767.1:n.-128del