Canonical Allele Identifier: CA438732339

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146485T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144863T>G , CM000666.2:g.25144863T>G	GRCh38
NC_000004.11:g.25146485T>G , CM000666.1:g.25146485T>G	GRCh37
NC_000004.10:g.24755583T>G	NCBI36
NG_028222.1:g.20720A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.937A>C MANE Select	ENSP00000371535.2:p.Arg313=
ENST00000680581.1:c.937A>C	ENSP00000506483.1:p.Arg313=
ENST00000680824.1:n.2153A>C
ENST00000681071.1:n.1229A>C
ENST00000681341.1:n.2078A>C
ENST00000681948.1:c.1192A>C	ENSP00000505991.1:p.Arg398=
ENST00000358971.7:c.*735A>C	ENSP00000351857.3:n.*735A>C
ENST00000382103.6:c.937A>C	ENSP00000371535.2:p.Arg313=
ENST00000503150.1:c.219A>C
ENST00000505513.1:n.237A>C
ENST00000514585.5:c.*638A>C	ENSP00000421880.1:n.*638A>C
NM_016955.3:c.937A>C	NP_058651.3:p.Arg313=
XM_005248168.2:c.700A>C	XP_005248225.1:p.Arg234=
XM_006713965.2:c.757A>C	XP_006714028.1:p.Arg253=
XM_011513846.1:c.934A>C	XP_011512148.1:p.Arg312=
XM_011513847.1:c.904A>C	XP_011512149.1:p.Arg302=
XM_011513848.1:c.757A>C	XP_011512150.1:p.Arg253=
XM_011513846.2:c.934A>C	XP_011512148.1:p.Arg312=
XM_011513847.2:c.904A>C	XP_011512149.1:p.Arg302=
XM_017008277.1:c.1192A>C	XP_016863766.1:p.Arg398=
XM_017008278.1:c.514A>C	XP_016863767.1:p.Arg172=
NM_016955.4:c.937A>C MANE Select	NP_058651.3:p.Arg313=