Canonical Allele Identifier: CA1060328038

Gene: SEPSECS

Linked Data

• gnomAD v3: 4-25156738-A-AAG
• gnomAD v4: 4-25156738-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156738_25156739insAG , CM000666.2:g.25156738_25156739insAG	GRCh38
NC_000004.11:g.25158360_25158361insAG , CM000666.1:g.25158360_25158361insAG	GRCh37
NC_000004.10:g.24767458_24767459insAG	NCBI36
NG_028222.1:g.8844_8845insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+117_388+118insCT MANE Select	ENSP00000371535.2:n.388+117_388+118insCT
ENST00000680581.1:c.388+117_388+118insCT	ENSP00000506483.1:n.388+117_388+118insCT
ENST00000680824.1:n.1604+117_1604+118insCT
ENST00000681071.1:n.680+117_680+118insCT
ENST00000681166.1:n.1435+117_1435+118insCT
ENST00000681341.1:n.1529+117_1529+118insCT
ENST00000681640.1:n.482+117_482+118insCT
ENST00000681948.1:c.643+117_643+118insCT	ENSP00000505991.1:n.643+117_643+118insCT
ENST00000358971.7:c.*186+117_*186+118insCT	ENSP00000351857.3:n.*186+117_*186+118insCT
ENST00000382103.6:c.388+117_388+118insCT	ENSP00000371535.2:n.388+117_388+118insCT
ENST00000514585.5:c.*89+117_*89+118insCT	ENSP00000421880.1:n.*89+117_*89+118insCT
NM_016955.3:c.388+117_388+118insCT	NP_058651.3:n.388+117_388+118insCT
XM_005248168.2:c.151+117_151+118insCT	XP_005248225.1:n.151+117_151+118insCT
XM_006713965.2:c.208+117_208+118insCT	XP_006714028.1:n.208+117_208+118insCT
XM_011513846.1:c.385+117_385+118insCT	XP_011512148.1:n.385+117_385+118insCT
XM_011513847.1:c.355+117_355+118insCT	XP_011512149.1:n.355+117_355+118insCT
XM_011513848.1:c.208+117_208+118insCT	XP_011512150.1:n.208+117_208+118insCT
XM_011513846.2:c.385+117_385+118insCT	XP_011512148.1:n.385+117_385+118insCT
XM_011513847.2:c.355+117_355+118insCT	XP_011512149.1:n.355+117_355+118insCT
XM_017008277.1:c.643+117_643+118insCT	XP_016863766.1:n.643+117_643+118insCT
XM_017008278.1:c.-36+117_-36+118insCT	XP_016863767.1:n.-36+117_-36+118insCT
NM_016955.4:c.388+117_388+118insCT MANE Select	NP_058651.3:n.388+117_388+118insCT