Canonical Allele Identifier: CA1445207722

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1712648119

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156500dup , CM000666.2:g.25156500dup	GRCh38
NC_000004.11:g.25158122dup , CM000666.1:g.25158122dup	GRCh37
NC_000004.10:g.24767220dup	NCBI36
NG_028222.1:g.9083dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.389-305dup MANE Select	ENSP00000371535.2:n.389-305dup
ENST00000680581.1:c.389-305dup	ENSP00000506483.1:n.389-305dup
ENST00000680824.1:n.1605-305dup
ENST00000681071.1:n.681-305dup
ENST00000681166.1:n.1436-305dup
ENST00000681341.1:n.1530-305dup
ENST00000681640.1:n.483-305dup
ENST00000681948.1:c.644-305dup	ENSP00000505991.1:n.644-305dup
ENST00000358971.7:c.*187-305dup	ENSP00000351857.3:n.*187-305dup
ENST00000382103.6:c.389-305dup	ENSP00000371535.2:n.389-305dup
ENST00000514585.5:c.*90-305dup	ENSP00000421880.1:n.*90-305dup
NM_016955.3:c.389-305dup	NP_058651.3:n.389-305dup
XM_005248168.2:c.152-305dup	XP_005248225.1:n.152-305dup
XM_006713965.2:c.209-305dup	XP_006714028.1:n.209-305dup
XM_011513846.1:c.386-305dup	XP_011512148.1:n.386-305dup
XM_011513847.1:c.356-305dup	XP_011512149.1:n.356-305dup
XM_011513848.1:c.209-305dup	XP_011512150.1:n.209-305dup
XM_011513846.2:c.386-305dup	XP_011512148.1:n.386-305dup
XM_011513847.2:c.356-305dup	XP_011512149.1:n.356-305dup
XM_017008277.1:c.644-305dup	XP_016863766.1:n.644-305dup
XM_017008278.1:c.-35-305dup	XP_016863767.1:n.-35-305dup
NM_016955.4:c.389-305dup MANE Select	NP_058651.3:n.389-305dup