Canonical Allele Identifier: CA438732704

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1712690980
• MyVariant Identifiers: chr4:g.25158494G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156872G>A , CM000666.2:g.25156872G>A	GRCh38
NC_000004.11:g.25158494G>A , CM000666.1:g.25158494G>A	GRCh37
NC_000004.10:g.24767592G>A	NCBI36
NG_028222.1:g.8711C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.372C>T MANE Select	ENSP00000371535.2:p.Asp124=
ENST00000680581.1:c.372C>T	ENSP00000506483.1:p.Asp124=
ENST00000680824.1:n.1588C>T
ENST00000681071.1:n.664C>T
ENST00000681166.1:n.1419C>T
ENST00000681341.1:n.1513C>T
ENST00000681640.1:n.466C>T
ENST00000681948.1:c.627C>T	ENSP00000505991.1:p.Asp209=
ENST00000358971.7:c.*170C>T	ENSP00000351857.3:n.*170C>T
ENST00000382103.6:c.372C>T	ENSP00000371535.2:p.Asp124=
ENST00000514585.5:c.*73C>T	ENSP00000421880.1:n.*73C>T
NM_016955.3:c.372C>T	NP_058651.3:p.Asp124=
XM_005248168.2:c.135C>T	XP_005248225.1:p.Asp45=
XM_006713965.2:c.192C>T	XP_006714028.1:p.Asp64=
XM_011513846.1:c.369C>T	XP_011512148.1:p.Asp123=
XM_011513847.1:c.339C>T	XP_011512149.1:p.Asp113=
XM_011513848.1:c.192C>T	XP_011512150.1:p.Asp64=
XM_011513846.2:c.369C>T	XP_011512148.1:p.Asp123=
XM_011513847.2:c.339C>T	XP_011512149.1:p.Asp113=
XM_017008277.1:c.627C>T	XP_016863766.1:p.Asp209=
XM_017008278.1:c.-52C>T	XP_016863767.1:n.-52C>T
NM_016955.4:c.372C>T MANE Select	NP_058651.3:p.Asp124=