Canonical Allele Identifier: CA438732768

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158578T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156956T>G , CM000666.2:g.25156956T>G	GRCh38
NC_000004.11:g.25158578T>G , CM000666.1:g.25158578T>G	GRCh37
NC_000004.10:g.24767676T>G	NCBI36
NG_028222.1:g.8627A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.288A>C MANE Select	ENSP00000371535.2:p.Gly96=
ENST00000680581.1:c.288A>C	ENSP00000506483.1:p.Gly96=
ENST00000680824.1:n.1504A>C
ENST00000681071.1:n.580A>C
ENST00000681166.1:n.1335A>C
ENST00000681341.1:n.1429A>C
ENST00000681640.1:n.382A>C
ENST00000681948.1:c.543A>C	ENSP00000505991.1:p.Gly181=
ENST00000358971.7:c.*86A>C	ENSP00000351857.3:n.*86A>C
ENST00000382103.6:c.288A>C	ENSP00000371535.2:p.Gly96=
ENST00000514585.5:c.133A>C	ENSP00000421880.1:p.Thr45Pro
NM_016955.3:c.288A>C	NP_058651.3:p.Gly96=
XM_005248168.2:c.51A>C	XP_005248225.1:p.Gly17=
XM_006713965.2:c.108A>C	XP_006714028.1:p.Gly36=
XM_011513846.1:c.285A>C	XP_011512148.1:p.Gly95=
XM_011513847.1:c.255A>C	XP_011512149.1:p.Gly85=
XM_011513848.1:c.108A>C	XP_011512150.1:p.Gly36=
XM_011513846.2:c.285A>C	XP_011512148.1:p.Gly95=
XM_011513847.2:c.255A>C	XP_011512149.1:p.Gly85=
XM_017008277.1:c.543A>C	XP_016863766.1:p.Gly181=
XM_017008278.1:c.-136A>C	XP_016863767.1:n.-136A>C
NM_016955.4:c.288A>C MANE Select	NP_058651.3:p.Gly96=