Canonical Allele Identifier: CA438732291

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146423G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144801G>T , CM000666.2:g.25144801G>T	GRCh38
NC_000004.11:g.25146423G>T , CM000666.1:g.25146423G>T	GRCh37
NC_000004.10:g.24755521G>T	NCBI36
NG_028222.1:g.20782C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.999C>A MANE Select	ENSP00000371535.2:p.Gly333=
ENST00000680581.1:c.999C>A	ENSP00000506483.1:p.Gly333=
ENST00000680824.1:n.2215C>A
ENST00000681071.1:n.1291C>A
ENST00000681341.1:n.2140C>A
ENST00000681948.1:c.1254C>A	ENSP00000505991.1:p.Gly418=
ENST00000358971.7:c.*797C>A	ENSP00000351857.3:n.*797C>A
ENST00000382103.6:c.999C>A	ENSP00000371535.2:p.Gly333=
ENST00000503150.1:c.281C>A
ENST00000505513.1:n.299C>A
ENST00000514585.5:c.*700C>A	ENSP00000421880.1:n.*700C>A
NM_016955.3:c.999C>A	NP_058651.3:p.Gly333=
XM_005248168.2:c.762C>A	XP_005248225.1:p.Gly254=
XM_006713965.2:c.819C>A	XP_006714028.1:p.Gly273=
XM_011513846.1:c.996C>A	XP_011512148.1:p.Gly332=
XM_011513847.1:c.966C>A	XP_011512149.1:p.Gly322=
XM_011513848.1:c.819C>A	XP_011512150.1:p.Gly273=
XM_011513846.2:c.996C>A	XP_011512148.1:p.Gly332=
XM_011513847.2:c.966C>A	XP_011512149.1:p.Gly322=
XM_017008277.1:c.1254C>A	XP_016863766.1:p.Gly418=
XM_017008278.1:c.576C>A	XP_016863767.1:p.Gly192=
NM_016955.4:c.999C>A MANE Select	NP_058651.3:p.Gly333=