Canonical Allele Identifier: CA356536971

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146481G>T (hg19) ; chr4:g.25144859G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144859G>T , CM000666.2:g.25144859G>T	GRCh38
NC_000004.11:g.25146481G>T , CM000666.1:g.25146481G>T	GRCh37
NC_000004.10:g.24755579G>T	NCBI36
NG_028222.1:g.20724C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.941C>A MANE Select	ENSP00000371535.2:p.Ala314Asp
ENST00000680581.1:c.941C>A	ENSP00000506483.1:p.Ala314Asp
ENST00000680824.1:n.2157C>A
ENST00000681071.1:n.1233C>A
ENST00000681341.1:n.2082C>A
ENST00000681948.1:c.1196C>A	ENSP00000505991.1:p.Ala399Asp
ENST00000358971.7:c.*739C>A	ENSP00000351857.3:n.*739C>A
ENST00000382103.6:c.941C>A	ENSP00000371535.2:p.Ala314Asp
ENST00000503150.1:c.223C>A
ENST00000505513.1:n.241C>A
ENST00000514585.5:c.*642C>A	ENSP00000421880.1:n.*642C>A
NM_016955.3:c.941C>A	NP_058651.3:p.Ala314Asp
XM_005248168.2:c.704C>A	XP_005248225.1:p.Ala235Asp
XM_006713965.2:c.761C>A	XP_006714028.1:p.Ala254Asp
XM_011513846.1:c.938C>A	XP_011512148.1:p.Ala313Asp
XM_011513847.1:c.908C>A	XP_011512149.1:p.Ala303Asp
XM_011513848.1:c.761C>A	XP_011512150.1:p.Ala254Asp
XM_011513846.2:c.938C>A	XP_011512148.1:p.Ala313Asp
XM_011513847.2:c.908C>A	XP_011512149.1:p.Ala303Asp
XM_017008277.1:c.1196C>A	XP_016863766.1:p.Ala399Asp
XM_017008278.1:c.518C>A	XP_016863767.1:p.Ala173Asp
NM_016955.4:c.941C>A MANE Select	NP_058651.3:p.Ala314Asp