Canonical Allele Identifier: CA2670197276

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156892-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156894del , CM000666.2:g.25156894del	GRCh38
NC_000004.11:g.25158516del , CM000666.1:g.25158516del	GRCh37
NC_000004.10:g.24767614del	NCBI36
NG_028222.1:g.8690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.351del MANE Select	ENSP00000371535.2:p.Thr118ProfsTer9
ENST00000680581.1:c.351del	ENSP00000506483.1:p.Thr118ProfsTer9
ENST00000680824.1:n.1567del
ENST00000681071.1:n.643del
ENST00000681166.1:n.1398del
ENST00000681341.1:n.1492del
ENST00000681640.1:n.445del
ENST00000681948.1:c.606del	ENSP00000505991.1:p.Thr203ProfsTer9
ENST00000358971.7:c.*149del	ENSP00000351857.3:n.*149del
ENST00000382103.6:c.351del	ENSP00000371535.2:p.Thr118ProfsTer9
ENST00000514585.5:c.*52del	ENSP00000421880.1:n.*52del
NM_016955.3:c.351del	NP_058651.3:p.Thr118ProfsTer9
XM_005248168.2:c.114del	XP_005248225.1:p.Thr39ProfsTer9
XM_006713965.2:c.171del	XP_006714028.1:p.Thr58ProfsTer9
XM_011513846.1:c.348del	XP_011512148.1:p.Thr117ProfsTer9
XM_011513847.1:c.318del	XP_011512149.1:p.Thr107ProfsTer9
XM_011513848.1:c.171del	XP_011512150.1:p.Thr58ProfsTer9
XM_011513846.2:c.348del	XP_011512148.1:p.Thr117ProfsTer9
XM_011513847.2:c.318del	XP_011512149.1:p.Thr107ProfsTer9
XM_017008277.1:c.606del	XP_016863766.1:p.Thr203ProfsTer9
XM_017008278.1:c.-73del	XP_016863767.1:n.-73del
NM_016955.4:c.351del MANE Select	NP_058651.3:p.Thr118ProfsTer9