Canonical Allele Identifier: CA356536810

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146440A>T (hg19) ; chr4:g.25144818A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144818A>T , CM000666.2:g.25144818A>T	GRCh38
NC_000004.11:g.25146440A>T , CM000666.1:g.25146440A>T	GRCh37
NC_000004.10:g.24755538A>T	NCBI36
NG_028222.1:g.20765T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.982T>A MANE Select	ENSP00000371535.2:p.Ser328Thr
ENST00000680581.1:c.982T>A	ENSP00000506483.1:p.Ser328Thr
ENST00000680824.1:n.2198T>A
ENST00000681071.1:n.1274T>A
ENST00000681341.1:n.2123T>A
ENST00000681948.1:c.1237T>A	ENSP00000505991.1:p.Ser413Thr
ENST00000358971.7:c.*780T>A	ENSP00000351857.3:n.*780T>A
ENST00000382103.6:c.982T>A	ENSP00000371535.2:p.Ser328Thr
ENST00000503150.1:c.264T>A
ENST00000505513.1:n.282T>A
ENST00000514585.5:c.*683T>A	ENSP00000421880.1:n.*683T>A
NM_016955.3:c.982T>A	NP_058651.3:p.Ser328Thr
XM_005248168.2:c.745T>A	XP_005248225.1:p.Ser249Thr
XM_006713965.2:c.802T>A	XP_006714028.1:p.Ser268Thr
XM_011513846.1:c.979T>A	XP_011512148.1:p.Ser327Thr
XM_011513847.1:c.949T>A	XP_011512149.1:p.Ser317Thr
XM_011513848.1:c.802T>A	XP_011512150.1:p.Ser268Thr
XM_011513846.2:c.979T>A	XP_011512148.1:p.Ser327Thr
XM_011513847.2:c.949T>A	XP_011512149.1:p.Ser317Thr
XM_017008277.1:c.1237T>A	XP_016863766.1:p.Ser413Thr
XM_017008278.1:c.559T>A	XP_016863767.1:p.Ser187Thr
NM_016955.4:c.982T>A MANE Select	NP_058651.3:p.Ser328Thr