Canonical Allele Identifier: CA438732319

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146459A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144837A>G , CM000666.2:g.25144837A>G	GRCh38
NC_000004.11:g.25146459A>G , CM000666.1:g.25146459A>G	GRCh37
NC_000004.10:g.24755557A>G	NCBI36
NG_028222.1:g.20746T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.963T>C MANE Select	ENSP00000371535.2:p.Asp321=
ENST00000680581.1:c.963T>C	ENSP00000506483.1:p.Asp321=
ENST00000680824.1:n.2179T>C
ENST00000681071.1:n.1255T>C
ENST00000681341.1:n.2104T>C
ENST00000681948.1:c.1218T>C	ENSP00000505991.1:p.Asp406=
ENST00000358971.7:c.*761T>C	ENSP00000351857.3:n.*761T>C
ENST00000382103.6:c.963T>C	ENSP00000371535.2:p.Asp321=
ENST00000503150.1:c.245T>C
ENST00000505513.1:n.263T>C
ENST00000514585.5:c.*664T>C	ENSP00000421880.1:n.*664T>C
NM_016955.3:c.963T>C	NP_058651.3:p.Asp321=
XM_005248168.2:c.726T>C	XP_005248225.1:p.Asp242=
XM_006713965.2:c.783T>C	XP_006714028.1:p.Asp261=
XM_011513846.1:c.960T>C	XP_011512148.1:p.Asp320=
XM_011513847.1:c.930T>C	XP_011512149.1:p.Asp310=
XM_011513848.1:c.783T>C	XP_011512150.1:p.Asp261=
XM_011513846.2:c.960T>C	XP_011512148.1:p.Asp320=
XM_011513847.2:c.930T>C	XP_011512149.1:p.Asp310=
XM_017008277.1:c.1218T>C	XP_016863766.1:p.Asp406=
XM_017008278.1:c.540T>C	XP_016863767.1:p.Asp180=
NM_016955.4:c.963T>C MANE Select	NP_058651.3:p.Asp321=