Canonical Allele Identifier: CA356542659

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158523T>C (hg19) ; chr4:g.25156901T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156901T>C , CM000666.2:g.25156901T>C	GRCh38
NC_000004.11:g.25158523T>C , CM000666.1:g.25158523T>C	GRCh37
NC_000004.10:g.24767621T>C	NCBI36
NG_028222.1:g.8682A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.343A>G MANE Select	ENSP00000371535.2:p.Asn115Asp
ENST00000680581.1:c.343A>G	ENSP00000506483.1:p.Asn115Asp
ENST00000680824.1:n.1559A>G
ENST00000681071.1:n.635A>G
ENST00000681166.1:n.1390A>G
ENST00000681341.1:n.1484A>G
ENST00000681640.1:n.437A>G
ENST00000681948.1:c.598A>G	ENSP00000505991.1:p.Asn200Asp
ENST00000358971.7:c.*141A>G	ENSP00000351857.3:n.*141A>G
ENST00000382103.6:c.343A>G	ENSP00000371535.2:p.Asn115Asp
ENST00000514585.5:c.*44A>G	ENSP00000421880.1:n.*44A>G
NM_016955.3:c.343A>G	NP_058651.3:p.Asn115Asp
XM_005248168.2:c.106A>G	XP_005248225.1:p.Asn36Asp
XM_006713965.2:c.163A>G	XP_006714028.1:p.Asn55Asp
XM_011513846.1:c.340A>G	XP_011512148.1:p.Asn114Asp
XM_011513847.1:c.310A>G	XP_011512149.1:p.Asn104Asp
XM_011513848.1:c.163A>G	XP_011512150.1:p.Asn55Asp
XM_011513846.2:c.340A>G	XP_011512148.1:p.Asn114Asp
XM_011513847.2:c.310A>G	XP_011512149.1:p.Asn104Asp
XM_017008277.1:c.598A>G	XP_016863766.1:p.Asn200Asp
XM_017008278.1:c.-81A>G	XP_016863767.1:n.-81A>G
NM_016955.4:c.343A>G MANE Select	NP_058651.3:p.Asn115Asp