Canonical Allele Identifier: CA438732334

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146477T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144855T>A , CM000666.2:g.25144855T>A	GRCh38
NC_000004.11:g.25146477T>A , CM000666.1:g.25146477T>A	GRCh37
NC_000004.10:g.24755575T>A	NCBI36
NG_028222.1:g.20728A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.945A>T MANE Select	ENSP00000371535.2:p.Ser315=
ENST00000680581.1:c.945A>T	ENSP00000506483.1:p.Ser315=
ENST00000680824.1:n.2161A>T
ENST00000681071.1:n.1237A>T
ENST00000681341.1:n.2086A>T
ENST00000681948.1:c.1200A>T	ENSP00000505991.1:p.Ser400=
ENST00000358971.7:c.*743A>T	ENSP00000351857.3:n.*743A>T
ENST00000382103.6:c.945A>T	ENSP00000371535.2:p.Ser315=
ENST00000503150.1:c.227A>T
ENST00000505513.1:n.245A>T
ENST00000514585.5:c.*646A>T	ENSP00000421880.1:n.*646A>T
NM_016955.3:c.945A>T	NP_058651.3:p.Ser315=
XM_005248168.2:c.708A>T	XP_005248225.1:p.Ser236=
XM_006713965.2:c.765A>T	XP_006714028.1:p.Ser255=
XM_011513846.1:c.942A>T	XP_011512148.1:p.Ser314=
XM_011513847.1:c.912A>T	XP_011512149.1:p.Ser304=
XM_011513848.1:c.765A>T	XP_011512150.1:p.Ser255=
XM_011513846.2:c.942A>T	XP_011512148.1:p.Ser314=
XM_011513847.2:c.912A>T	XP_011512149.1:p.Ser304=
XM_017008277.1:c.1200A>T	XP_016863766.1:p.Ser400=
XM_017008278.1:c.522A>T	XP_016863767.1:p.Ser174=
NM_016955.4:c.945A>T MANE Select	NP_058651.3:p.Ser315=