Canonical Allele Identifier: CA2670197245

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156802-G-GGTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156813_25156816dup , CM000666.2:g.25156813_25156816dup	GRCh38
NC_000004.11:g.25158435_25158438dup , CM000666.1:g.25158435_25158438dup	GRCh37
NC_000004.10:g.24767533_24767536dup	NCBI36
NG_028222.1:g.8777_8780dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.388+50_388+53dup MANE Select	ENSP00000371535.2:n.388+50_388+53dup
ENST00000680581.1:c.388+50_388+53dup	ENSP00000506483.1:n.388+50_388+53dup
ENST00000680824.1:n.1604+50_1604+53dup
ENST00000681071.1:n.680+50_680+53dup
ENST00000681166.1:n.1435+50_1435+53dup
ENST00000681341.1:n.1529+50_1529+53dup
ENST00000681640.1:n.482+50_482+53dup
ENST00000681948.1:c.643+50_643+53dup	ENSP00000505991.1:n.643+50_643+53dup
ENST00000358971.7:c.*186+50_*186+53dup	ENSP00000351857.3:n.*186+50_*186+53dup
ENST00000382103.6:c.388+50_388+53dup	ENSP00000371535.2:n.388+50_388+53dup
ENST00000514585.5:c.*89+50_*89+53dup	ENSP00000421880.1:n.*89+50_*89+53dup
NM_016955.3:c.388+50_388+53dup	NP_058651.3:n.388+50_388+53dup
XM_005248168.2:c.151+50_151+53dup	XP_005248225.1:n.151+50_151+53dup
XM_006713965.2:c.208+50_208+53dup	XP_006714028.1:n.208+50_208+53dup
XM_011513846.1:c.385+50_385+53dup	XP_011512148.1:n.385+50_385+53dup
XM_011513847.1:c.355+50_355+53dup	XP_011512149.1:n.355+50_355+53dup
XM_011513848.1:c.208+50_208+53dup	XP_011512150.1:n.208+50_208+53dup
XM_011513846.2:c.385+50_385+53dup	XP_011512148.1:n.385+50_385+53dup
XM_011513847.2:c.355+50_355+53dup	XP_011512149.1:n.355+50_355+53dup
XM_017008277.1:c.643+50_643+53dup	XP_016863766.1:n.643+50_643+53dup
XM_017008278.1:c.-36+50_-36+53dup	XP_016863767.1:n.-36+50_-36+53dup
NM_016955.4:c.388+50_388+53dup MANE Select	NP_058651.3:n.388+50_388+53dup