Canonical Allele Identifier: CA2670197209

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156754-ACTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156755_25156757del , CM000666.2:g.25156755_25156757del	GRCh38
NC_000004.11:g.25158377_25158379del , CM000666.1:g.25158377_25158379del	GRCh37
NC_000004.10:g.24767475_24767477del	NCBI36
NG_028222.1:g.8826_8828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+99_388+101del MANE Select	ENSP00000371535.2:n.388+99_388+101del
ENST00000680581.1:c.388+99_388+101del	ENSP00000506483.1:n.388+99_388+101del
ENST00000680824.1:n.1604+99_1604+101del
ENST00000681071.1:n.680+99_680+101del
ENST00000681166.1:n.1435+99_1435+101del
ENST00000681341.1:n.1529+99_1529+101del
ENST00000681640.1:n.482+99_482+101del
ENST00000681948.1:c.643+99_643+101del	ENSP00000505991.1:n.643+99_643+101del
ENST00000358971.7:c.*186+99_*186+101del	ENSP00000351857.3:n.*186+99_*186+101del
ENST00000382103.6:c.388+99_388+101del	ENSP00000371535.2:n.388+99_388+101del
ENST00000514585.5:c.*89+99_*89+101del	ENSP00000421880.1:n.*89+99_*89+101del
NM_016955.3:c.388+99_388+101del	NP_058651.3:n.388+99_388+101del
XM_005248168.2:c.151+99_151+101del	XP_005248225.1:n.151+99_151+101del
XM_006713965.2:c.208+99_208+101del	XP_006714028.1:n.208+99_208+101del
XM_011513846.1:c.385+99_385+101del	XP_011512148.1:n.385+99_385+101del
XM_011513847.1:c.355+99_355+101del	XP_011512149.1:n.355+99_355+101del
XM_011513848.1:c.208+99_208+101del	XP_011512150.1:n.208+99_208+101del
XM_011513846.2:c.385+99_385+101del	XP_011512148.1:n.385+99_385+101del
XM_011513847.2:c.355+99_355+101del	XP_011512149.1:n.355+99_355+101del
XM_017008277.1:c.643+99_643+101del	XP_016863766.1:n.643+99_643+101del
XM_017008278.1:c.-36+99_-36+101del	XP_016863767.1:n.-36+99_-36+101del
NM_016955.4:c.388+99_388+101del MANE Select	NP_058651.3:n.388+99_388+101del