Canonical Allele Identifier: CA2670197147

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156720-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156720_25156721insG , CM000666.2:g.25156720_25156721insG	GRCh38
NC_000004.11:g.25158342_25158343insG , CM000666.1:g.25158342_25158343insG	GRCh37
NC_000004.10:g.24767440_24767441insG	NCBI36
NG_028222.1:g.8862_8863insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+135_388+136insC MANE Select	ENSP00000371535.2:n.388+135_388+136insC
ENST00000680581.1:c.388+135_388+136insC	ENSP00000506483.1:n.388+135_388+136insC
ENST00000680824.1:n.1604+135_1604+136insC
ENST00000681071.1:n.680+135_680+136insC
ENST00000681166.1:n.1435+135_1435+136insC
ENST00000681341.1:n.1529+135_1529+136insC
ENST00000681640.1:n.482+135_482+136insC
ENST00000681948.1:c.643+135_643+136insC	ENSP00000505991.1:n.643+135_643+136insC
ENST00000358971.7:c.*186+135_*186+136insC	ENSP00000351857.3:n.*186+135_*186+136insC
ENST00000382103.6:c.388+135_388+136insC	ENSP00000371535.2:n.388+135_388+136insC
ENST00000514585.5:c.*89+135_*89+136insC	ENSP00000421880.1:n.*89+135_*89+136insC
NM_016955.3:c.388+135_388+136insC	NP_058651.3:n.388+135_388+136insC
XM_005248168.2:c.151+135_151+136insC	XP_005248225.1:n.151+135_151+136insC
XM_006713965.2:c.208+135_208+136insC	XP_006714028.1:n.208+135_208+136insC
XM_011513846.1:c.385+135_385+136insC	XP_011512148.1:n.385+135_385+136insC
XM_011513847.1:c.355+135_355+136insC	XP_011512149.1:n.355+135_355+136insC
XM_011513848.1:c.208+135_208+136insC	XP_011512150.1:n.208+135_208+136insC
XM_011513846.2:c.385+135_385+136insC	XP_011512148.1:n.385+135_385+136insC
XM_011513847.2:c.355+135_355+136insC	XP_011512149.1:n.355+135_355+136insC
XM_017008277.1:c.643+135_643+136insC	XP_016863766.1:n.643+135_643+136insC
XM_017008278.1:c.-36+135_-36+136insC	XP_016863767.1:n.-36+135_-36+136insC
NM_016955.4:c.388+135_388+136insC MANE Select	NP_058651.3:n.388+135_388+136insC