Canonical Allele Identifier: CA1445207444

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1712634633

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156371G>A , CM000666.2:g.25156371G>A	GRCh38
NC_000004.11:g.25157993G>A , CM000666.1:g.25157993G>A	GRCh37
NC_000004.10:g.24767091G>A	NCBI36
NG_028222.1:g.9212C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.389-176C>T MANE Select	ENSP00000371535.2:n.389-176C>T
ENST00000680581.1:c.389-176C>T	ENSP00000506483.1:n.389-176C>T
ENST00000680824.1:n.1605-176C>T
ENST00000681071.1:n.681-176C>T
ENST00000681166.1:n.1436-176C>T
ENST00000681341.1:n.1530-176C>T
ENST00000681640.1:n.483-176C>T
ENST00000681948.1:c.644-176C>T	ENSP00000505991.1:n.644-176C>T
ENST00000358971.7:c.*187-176C>T	ENSP00000351857.3:n.*187-176C>T
ENST00000382103.6:c.389-176C>T	ENSP00000371535.2:n.389-176C>T
ENST00000514585.5:c.*90-176C>T	ENSP00000421880.1:n.*90-176C>T
NM_016955.3:c.389-176C>T	NP_058651.3:n.389-176C>T
XM_005248168.2:c.152-176C>T	XP_005248225.1:n.152-176C>T
XM_006713965.2:c.209-176C>T	XP_006714028.1:n.209-176C>T
XM_011513846.1:c.386-176C>T	XP_011512148.1:n.386-176C>T
XM_011513847.1:c.356-176C>T	XP_011512149.1:n.356-176C>T
XM_011513848.1:c.209-176C>T	XP_011512150.1:n.209-176C>T
XM_011513846.2:c.386-176C>T	XP_011512148.1:n.386-176C>T
XM_011513847.2:c.356-176C>T	XP_011512149.1:n.356-176C>T
XM_017008277.1:c.644-176C>T	XP_016863766.1:n.644-176C>T
XM_017008278.1:c.-35-176C>T	XP_016863767.1:n.-35-176C>T
NM_016955.4:c.389-176C>T MANE Select	NP_058651.3:n.389-176C>T