Canonical Allele Identifier: CA1445208451

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1712676030

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156731_25156732insGA , CM000666.2:g.25156731_25156732insGA	GRCh38
NC_000004.11:g.25158353_25158354insGA , CM000666.1:g.25158353_25158354insGA	GRCh37
NC_000004.10:g.24767451_24767452insGA	NCBI36
NG_028222.1:g.8852_8853insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+125_388+126insCT MANE Select	ENSP00000371535.2:n.388+125_388+126insCT
ENST00000680581.1:c.388+125_388+126insCT	ENSP00000506483.1:n.388+125_388+126insCT
ENST00000680824.1:n.1604+125_1604+126insCT
ENST00000681071.1:n.680+125_680+126insCT
ENST00000681166.1:n.1435+125_1435+126insCT
ENST00000681341.1:n.1529+125_1529+126insCT
ENST00000681640.1:n.482+125_482+126insCT
ENST00000681948.1:c.643+125_643+126insCT	ENSP00000505991.1:n.643+125_643+126insCT
ENST00000358971.7:c.*186+125_*186+126insCT	ENSP00000351857.3:n.*186+125_*186+126insCT
ENST00000382103.6:c.388+125_388+126insCT	ENSP00000371535.2:n.388+125_388+126insCT
ENST00000514585.5:c.*89+125_*89+126insCT	ENSP00000421880.1:n.*89+125_*89+126insCT
NM_016955.3:c.388+125_388+126insCT	NP_058651.3:n.388+125_388+126insCT
XM_005248168.2:c.151+125_151+126insCT	XP_005248225.1:n.151+125_151+126insCT
XM_006713965.2:c.208+125_208+126insCT	XP_006714028.1:n.208+125_208+126insCT
XM_011513846.1:c.385+125_385+126insCT	XP_011512148.1:n.385+125_385+126insCT
XM_011513847.1:c.355+125_355+126insCT	XP_011512149.1:n.355+125_355+126insCT
XM_011513848.1:c.208+125_208+126insCT	XP_011512150.1:n.208+125_208+126insCT
XM_011513846.2:c.385+125_385+126insCT	XP_011512148.1:n.385+125_385+126insCT
XM_011513847.2:c.355+125_355+126insCT	XP_011512149.1:n.355+125_355+126insCT
XM_017008277.1:c.643+125_643+126insCT	XP_016863766.1:n.643+125_643+126insCT
XM_017008278.1:c.-36+125_-36+126insCT	XP_016863767.1:n.-36+125_-36+126insCT
NM_016955.4:c.388+125_388+126insCT MANE Select	NP_058651.3:n.388+125_388+126insCT