Canonical Allele Identifier: CA356536741

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146422A>T (hg19) ; chr4:g.25144800A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144800A>T , CM000666.2:g.25144800A>T	GRCh38
NC_000004.11:g.25146422A>T , CM000666.1:g.25146422A>T	GRCh37
NC_000004.10:g.24755520A>T	NCBI36
NG_028222.1:g.20783T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.1000T>A MANE Select	ENSP00000371535.2:p.Tyr334Asn
ENST00000680581.1:c.1000T>A	ENSP00000506483.1:p.Tyr334Asn
ENST00000680824.1:n.2216T>A
ENST00000681071.1:n.1292T>A
ENST00000681341.1:n.2141T>A
ENST00000681948.1:c.1255T>A	ENSP00000505991.1:p.Tyr419Asn
ENST00000358971.7:c.*798T>A	ENSP00000351857.3:n.*798T>A
ENST00000382103.6:c.1000T>A	ENSP00000371535.2:p.Tyr334Asn
ENST00000503150.1:c.282T>A
ENST00000505513.1:n.300T>A
ENST00000514585.5:c.*701T>A	ENSP00000421880.1:n.*701T>A
NM_016955.3:c.1000T>A	NP_058651.3:p.Tyr334Asn
XM_005248168.2:c.763T>A	XP_005248225.1:p.Tyr255Asn
XM_006713965.2:c.820T>A	XP_006714028.1:p.Tyr274Asn
XM_011513846.1:c.997T>A	XP_011512148.1:p.Tyr333Asn
XM_011513847.1:c.967T>A	XP_011512149.1:p.Tyr323Asn
XM_011513848.1:c.820T>A	XP_011512150.1:p.Tyr274Asn
XM_011513846.2:c.997T>A	XP_011512148.1:p.Tyr333Asn
XM_011513847.2:c.967T>A	XP_011512149.1:p.Tyr323Asn
XM_017008277.1:c.1255T>A	XP_016863766.1:p.Tyr419Asn
XM_017008278.1:c.577T>A	XP_016863767.1:p.Tyr193Asn
NM_016955.4:c.1000T>A MANE Select	NP_058651.3:p.Tyr334Asn