Canonical Allele Identifier: CA356542602

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158511T>A (hg19) ; chr4:g.25156889T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156889T>A , CM000666.2:g.25156889T>A	GRCh38
NC_000004.11:g.25158511T>A , CM000666.1:g.25158511T>A	GRCh37
NC_000004.10:g.24767609T>A	NCBI36
NG_028222.1:g.8694A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.355A>T MANE Select	ENSP00000371535.2:p.Asn119Tyr
ENST00000680581.1:c.355A>T	ENSP00000506483.1:p.Asn119Tyr
ENST00000680824.1:n.1571A>T
ENST00000681071.1:n.647A>T
ENST00000681166.1:n.1402A>T
ENST00000681341.1:n.1496A>T
ENST00000681640.1:n.449A>T
ENST00000681948.1:c.610A>T	ENSP00000505991.1:p.Asn204Tyr
ENST00000358971.7:c.*153A>T	ENSP00000351857.3:n.*153A>T
ENST00000382103.6:c.355A>T	ENSP00000371535.2:p.Asn119Tyr
ENST00000514585.5:c.*56A>T	ENSP00000421880.1:n.*56A>T
NM_016955.3:c.355A>T	NP_058651.3:p.Asn119Tyr
XM_005248168.2:c.118A>T	XP_005248225.1:p.Asn40Tyr
XM_006713965.2:c.175A>T	XP_006714028.1:p.Asn59Tyr
XM_011513846.1:c.352A>T	XP_011512148.1:p.Asn118Tyr
XM_011513847.1:c.322A>T	XP_011512149.1:p.Asn108Tyr
XM_011513848.1:c.175A>T	XP_011512150.1:p.Asn59Tyr
XM_011513846.2:c.352A>T	XP_011512148.1:p.Asn118Tyr
XM_011513847.2:c.322A>T	XP_011512149.1:p.Asn108Tyr
XM_017008277.1:c.610A>T	XP_016863766.1:p.Asn204Tyr
XM_017008278.1:c.-69A>T	XP_016863767.1:n.-69A>T
NM_016955.4:c.355A>T MANE Select	NP_058651.3:p.Asn119Tyr