Canonical Allele Identifier: CA2760775139

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156744_25156745dup , CM000666.2:g.25156744_25156745dup	GRCh38
NC_000004.11:g.25158366_25158367dup , CM000666.1:g.25158366_25158367dup	GRCh37
NC_000004.10:g.24767464_24767465dup	NCBI36
NG_028222.1:g.8840_8841dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+113_388+114dup MANE Select	ENSP00000371535.2:n.388+113_388+114dup
ENST00000680581.1:c.388+113_388+114dup	ENSP00000506483.1:n.388+113_388+114dup
ENST00000680824.1:n.1604+113_1604+114dup
ENST00000681071.1:n.680+113_680+114dup
ENST00000681166.1:n.1435+113_1435+114dup
ENST00000681341.1:n.1529+113_1529+114dup
ENST00000681640.1:n.482+113_482+114dup
ENST00000681948.1:c.643+113_643+114dup	ENSP00000505991.1:n.643+113_643+114dup
ENST00000358971.7:c.*186+113_*186+114dup	ENSP00000351857.3:n.*186+113_*186+114dup
ENST00000382103.6:c.388+113_388+114dup	ENSP00000371535.2:n.388+113_388+114dup
ENST00000514585.5:c.*89+113_*89+114dup	ENSP00000421880.1:n.*89+113_*89+114dup
NM_016955.3:c.388+113_388+114dup	NP_058651.3:n.388+113_388+114dup
XM_005248168.2:c.151+113_151+114dup	XP_005248225.1:n.151+113_151+114dup
XM_006713965.2:c.208+113_208+114dup	XP_006714028.1:n.208+113_208+114dup
XM_011513846.1:c.385+113_385+114dup	XP_011512148.1:n.385+113_385+114dup
XM_011513847.1:c.355+113_355+114dup	XP_011512149.1:n.355+113_355+114dup
XM_011513848.1:c.208+113_208+114dup	XP_011512150.1:n.208+113_208+114dup
XM_011513846.2:c.385+113_385+114dup	XP_011512148.1:n.385+113_385+114dup
XM_011513847.2:c.355+113_355+114dup	XP_011512149.1:n.355+113_355+114dup
XM_017008277.1:c.643+113_643+114dup	XP_016863766.1:n.643+113_643+114dup
XM_017008278.1:c.-36+113_-36+114dup	XP_016863767.1:n.-36+113_-36+114dup
NM_016955.4:c.388+113_388+114dup MANE Select	NP_058651.3:n.388+113_388+114dup