Canonical Allele Identifier: CA2670197274

Gene: SEPSECS

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156855_25156856dup , CM000666.2:g.25156855_25156856dup	GRCh38
NC_000004.11:g.25158477_25158478dup , CM000666.1:g.25158477_25158478dup	GRCh37
NC_000004.10:g.24767575_24767576dup	NCBI36
NG_028222.1:g.8727_8728dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388_388+1dup
ENST00000680581.1:c.388_388+1dup
ENST00000680824.1:n.1604_1604+1dup
ENST00000681071.1:n.680_680+1dup
ENST00000681166.1:n.1435_1435+1dup
ENST00000681341.1:n.1529_1529+1dup
ENST00000681640.1:n.482_482+1dup
ENST00000681948.1:c.643_643+1dup
ENST00000358971.7:c.*186_*186+1dup
ENST00000382103.6:c.388_388+1dup
ENST00000514585.5:c.*89_*89+1dup
NM_016955.3:c.388_388+1dup
XM_005248168.2:c.151_151+1dup
XM_006713965.2:c.208_208+1dup
XM_011513846.1:c.385_385+1dup
XM_011513847.1:c.355_355+1dup
XM_011513848.1:c.208_208+1dup
XM_011513846.2:c.385_385+1dup
XM_011513847.2:c.355_355+1dup
XM_017008277.1:c.643_643+1dup
XM_017008278.1:c.-36_-36+1dup
NM_016955.4:c.388_388+1dup