Canonical Allele Identifier: CA1445208557

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1712682270
• gnomAD v4: 4-25156781-T-TAATAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156783_25156787dup , CM000666.2:g.25156783_25156787dup	GRCh38
NC_000004.11:g.25158405_25158409dup , CM000666.1:g.25158405_25158409dup	GRCh37
NC_000004.10:g.24767503_24767507dup	NCBI36
NG_028222.1:g.8797_8801dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.388+70_388+74dup MANE Select	ENSP00000371535.2:n.388+70_388+74dup
ENST00000680581.1:c.388+70_388+74dup	ENSP00000506483.1:n.388+70_388+74dup
ENST00000680824.1:n.1604+70_1604+74dup
ENST00000681071.1:n.680+70_680+74dup
ENST00000681166.1:n.1435+70_1435+74dup
ENST00000681341.1:n.1529+70_1529+74dup
ENST00000681640.1:n.482+70_482+74dup
ENST00000681948.1:c.643+70_643+74dup	ENSP00000505991.1:n.643+70_643+74dup
ENST00000358971.7:c.*186+70_*186+74dup	ENSP00000351857.3:n.*186+70_*186+74dup
ENST00000382103.6:c.388+70_388+74dup	ENSP00000371535.2:n.388+70_388+74dup
ENST00000514585.5:c.*89+70_*89+74dup	ENSP00000421880.1:n.*89+70_*89+74dup
NM_016955.3:c.388+70_388+74dup	NP_058651.3:n.388+70_388+74dup
XM_005248168.2:c.151+70_151+74dup	XP_005248225.1:n.151+70_151+74dup
XM_006713965.2:c.208+70_208+74dup	XP_006714028.1:n.208+70_208+74dup
XM_011513846.1:c.385+70_385+74dup	XP_011512148.1:n.385+70_385+74dup
XM_011513847.1:c.355+70_355+74dup	XP_011512149.1:n.355+70_355+74dup
XM_011513848.1:c.208+70_208+74dup	XP_011512150.1:n.208+70_208+74dup
XM_011513846.2:c.385+70_385+74dup	XP_011512148.1:n.385+70_385+74dup
XM_011513847.2:c.355+70_355+74dup	XP_011512149.1:n.355+70_355+74dup
XM_017008277.1:c.643+70_643+74dup	XP_016863766.1:n.643+70_643+74dup
XM_017008278.1:c.-36+70_-36+74dup	XP_016863767.1:n.-36+70_-36+74dup
NM_016955.4:c.388+70_388+74dup MANE Select	NP_058651.3:n.388+70_388+74dup