Canonical Allele Identifier: CA2670197187

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156737-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156737_25156738insTT , CM000666.2:g.25156737_25156738insTT	GRCh38
NC_000004.11:g.25158359_25158360insTT , CM000666.1:g.25158359_25158360insTT	GRCh37
NC_000004.10:g.24767457_24767458insTT	NCBI36
NG_028222.1:g.8845_8846insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+118_388+119insAA MANE Select	ENSP00000371535.2:n.388+118_388+119insAA
ENST00000680581.1:c.388+118_388+119insAA	ENSP00000506483.1:n.388+118_388+119insAA
ENST00000680824.1:n.1604+118_1604+119insAA
ENST00000681071.1:n.680+118_680+119insAA
ENST00000681166.1:n.1435+118_1435+119insAA
ENST00000681341.1:n.1529+118_1529+119insAA
ENST00000681640.1:n.482+118_482+119insAA
ENST00000681948.1:c.643+118_643+119insAA	ENSP00000505991.1:n.643+118_643+119insAA
ENST00000358971.7:c.*186+118_*186+119insAA	ENSP00000351857.3:n.*186+118_*186+119insAA
ENST00000382103.6:c.388+118_388+119insAA	ENSP00000371535.2:n.388+118_388+119insAA
ENST00000514585.5:c.*89+118_*89+119insAA	ENSP00000421880.1:n.*89+118_*89+119insAA
NM_016955.3:c.388+118_388+119insAA	NP_058651.3:n.388+118_388+119insAA
XM_005248168.2:c.151+118_151+119insAA	XP_005248225.1:n.151+118_151+119insAA
XM_006713965.2:c.208+118_208+119insAA	XP_006714028.1:n.208+118_208+119insAA
XM_011513846.1:c.385+118_385+119insAA	XP_011512148.1:n.385+118_385+119insAA
XM_011513847.1:c.355+118_355+119insAA	XP_011512149.1:n.355+118_355+119insAA
XM_011513848.1:c.208+118_208+119insAA	XP_011512150.1:n.208+118_208+119insAA
XM_011513846.2:c.385+118_385+119insAA	XP_011512148.1:n.385+118_385+119insAA
XM_011513847.2:c.355+118_355+119insAA	XP_011512149.1:n.355+118_355+119insAA
XM_017008277.1:c.643+118_643+119insAA	XP_016863766.1:n.643+118_643+119insAA
XM_017008278.1:c.-36+118_-36+119insAA	XP_016863767.1:n.-36+118_-36+119insAA
NM_016955.4:c.388+118_388+119insAA MANE Select	NP_058651.3:n.388+118_388+119insAA