Canonical Allele Identifier: CA356536950

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146475G>T (hg19) ; chr4:g.25144853G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144853G>T , CM000666.2:g.25144853G>T	GRCh38
NC_000004.11:g.25146475G>T , CM000666.1:g.25146475G>T	GRCh37
NC_000004.10:g.24755573G>T	NCBI36
NG_028222.1:g.20730C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.947C>A MANE Select	ENSP00000371535.2:p.Ala316Asp
ENST00000680581.1:c.947C>A	ENSP00000506483.1:p.Ala316Asp
ENST00000680824.1:n.2163C>A
ENST00000681071.1:n.1239C>A
ENST00000681341.1:n.2088C>A
ENST00000681948.1:c.1202C>A	ENSP00000505991.1:p.Ala401Asp
ENST00000358971.7:c.*745C>A	ENSP00000351857.3:n.*745C>A
ENST00000382103.6:c.947C>A	ENSP00000371535.2:p.Ala316Asp
ENST00000503150.1:c.229C>A
ENST00000505513.1:n.247C>A
ENST00000514585.5:c.*648C>A	ENSP00000421880.1:n.*648C>A
NM_016955.3:c.947C>A	NP_058651.3:p.Ala316Asp
XM_005248168.2:c.710C>A	XP_005248225.1:p.Ala237Asp
XM_006713965.2:c.767C>A	XP_006714028.1:p.Ala256Asp
XM_011513846.1:c.944C>A	XP_011512148.1:p.Ala315Asp
XM_011513847.1:c.914C>A	XP_011512149.1:p.Ala305Asp
XM_011513848.1:c.767C>A	XP_011512150.1:p.Ala256Asp
XM_011513846.2:c.944C>A	XP_011512148.1:p.Ala315Asp
XM_011513847.2:c.914C>A	XP_011512149.1:p.Ala305Asp
XM_017008277.1:c.1202C>A	XP_016863766.1:p.Ala401Asp
XM_017008278.1:c.524C>A	XP_016863767.1:p.Ala175Asp
NM_016955.4:c.947C>A MANE Select	NP_058651.3:p.Ala316Asp