Canonical Allele Identifier: CA356536968

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146479A>T (hg19) ; chr4:g.25144857A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144857A>T , CM000666.2:g.25144857A>T	GRCh38
NC_000004.11:g.25146479A>T , CM000666.1:g.25146479A>T	GRCh37
NC_000004.10:g.24755577A>T	NCBI36
NG_028222.1:g.20726T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.943T>A MANE Select	ENSP00000371535.2:p.Ser315Thr
ENST00000680581.1:c.943T>A	ENSP00000506483.1:p.Ser315Thr
ENST00000680824.1:n.2159T>A
ENST00000681071.1:n.1235T>A
ENST00000681341.1:n.2084T>A
ENST00000681948.1:c.1198T>A	ENSP00000505991.1:p.Ser400Thr
ENST00000358971.7:c.*741T>A	ENSP00000351857.3:n.*741T>A
ENST00000382103.6:c.943T>A	ENSP00000371535.2:p.Ser315Thr
ENST00000503150.1:c.225T>A
ENST00000505513.1:n.243T>A
ENST00000514585.5:c.*644T>A	ENSP00000421880.1:n.*644T>A
NM_016955.3:c.943T>A	NP_058651.3:p.Ser315Thr
XM_005248168.2:c.706T>A	XP_005248225.1:p.Ser236Thr
XM_006713965.2:c.763T>A	XP_006714028.1:p.Ser255Thr
XM_011513846.1:c.940T>A	XP_011512148.1:p.Ser314Thr
XM_011513847.1:c.910T>A	XP_011512149.1:p.Ser304Thr
XM_011513848.1:c.763T>A	XP_011512150.1:p.Ser255Thr
XM_011513846.2:c.940T>A	XP_011512148.1:p.Ser314Thr
XM_011513847.2:c.910T>A	XP_011512149.1:p.Ser304Thr
XM_017008277.1:c.1198T>A	XP_016863766.1:p.Ser400Thr
XM_017008278.1:c.520T>A	XP_016863767.1:p.Ser174Thr
NM_016955.4:c.943T>A MANE Select	NP_058651.3:p.Ser315Thr