Canonical Allele Identifier: CA356536808

Gene: SEPSECS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.982T>G MANE Select	ENSP00000371535.2:p.Ser328Ala
ENST00000680581.1:c.982T>G	ENSP00000506483.1:p.Ser328Ala
ENST00000680824.1:n.2198T>G
ENST00000681071.1:n.1274T>G
ENST00000681341.1:n.2123T>G
ENST00000681948.1:c.1237T>G	ENSP00000505991.1:p.Ser413Ala
ENST00000358971.7:c.*780T>G	ENSP00000351857.3:n.*780T>G
ENST00000382103.6:c.982T>G	ENSP00000371535.2:p.Ser328Ala
ENST00000503150.1:c.264T>G
ENST00000505513.1:n.282T>G
ENST00000514585.5:c.*683T>G	ENSP00000421880.1:n.*683T>G
NM_016955.3:c.982T>G	NP_058651.3:p.Ser328Ala
XM_005248168.2:c.745T>G	XP_005248225.1:p.Ser249Ala
XM_006713965.2:c.802T>G	XP_006714028.1:p.Ser268Ala
XM_011513846.1:c.979T>G	XP_011512148.1:p.Ser327Ala
XM_011513847.1:c.949T>G	XP_011512149.1:p.Ser317Ala
XM_011513848.1:c.802T>G	XP_011512150.1:p.Ser268Ala
XM_011513846.2:c.979T>G	XP_011512148.1:p.Ser327Ala
XM_011513847.2:c.949T>G	XP_011512149.1:p.Ser317Ala
XM_017008277.1:c.1237T>G	XP_016863766.1:p.Ser413Ala
XM_017008278.1:c.559T>G	XP_016863767.1:p.Ser187Ala
NM_016955.4:c.982T>G MANE Select	NP_058651.3:p.Ser328Ala