Canonical Allele Identifier: CA438732296

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146432T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144810T>A , CM000666.2:g.25144810T>A	GRCh38
NC_000004.11:g.25146432T>A , CM000666.1:g.25146432T>A	GRCh37
NC_000004.10:g.24755530T>A	NCBI36
NG_028222.1:g.20773A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.990A>T MANE Select	ENSP00000371535.2:p.Gly330=
ENST00000680581.1:c.990A>T	ENSP00000506483.1:p.Gly330=
ENST00000680824.1:n.2206A>T
ENST00000681071.1:n.1282A>T
ENST00000681341.1:n.2131A>T
ENST00000681948.1:c.1245A>T	ENSP00000505991.1:p.Gly415=
ENST00000358971.7:c.*788A>T	ENSP00000351857.3:n.*788A>T
ENST00000382103.6:c.990A>T	ENSP00000371535.2:p.Gly330=
ENST00000503150.1:c.272A>T
ENST00000505513.1:n.290A>T
ENST00000514585.5:c.*691A>T	ENSP00000421880.1:n.*691A>T
NM_016955.3:c.990A>T	NP_058651.3:p.Gly330=
XM_005248168.2:c.753A>T	XP_005248225.1:p.Gly251=
XM_006713965.2:c.810A>T	XP_006714028.1:p.Gly270=
XM_011513846.1:c.987A>T	XP_011512148.1:p.Gly329=
XM_011513847.1:c.957A>T	XP_011512149.1:p.Gly319=
XM_011513848.1:c.810A>T	XP_011512150.1:p.Gly270=
XM_011513846.2:c.987A>T	XP_011512148.1:p.Gly329=
XM_011513847.2:c.957A>T	XP_011512149.1:p.Gly319=
XM_017008277.1:c.1245A>T	XP_016863766.1:p.Gly415=
XM_017008278.1:c.567A>T	XP_016863767.1:p.Gly189=
NM_016955.4:c.990A>T MANE Select	NP_058651.3:p.Gly330=