Canonical Allele Identifier: CA356536915

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146466G>T (hg19) ; chr4:g.25144844G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144844G>T , CM000666.2:g.25144844G>T	GRCh38
NC_000004.11:g.25146466G>T , CM000666.1:g.25146466G>T	GRCh37
NC_000004.10:g.24755564G>T	NCBI36
NG_028222.1:g.20739C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.956C>A MANE Select	ENSP00000371535.2:p.Ser319Tyr
ENST00000680581.1:c.956C>A	ENSP00000506483.1:p.Ser319Tyr
ENST00000680824.1:n.2172C>A
ENST00000681071.1:n.1248C>A
ENST00000681341.1:n.2097C>A
ENST00000681948.1:c.1211C>A	ENSP00000505991.1:p.Ser404Tyr
ENST00000358971.7:c.*754C>A	ENSP00000351857.3:n.*754C>A
ENST00000382103.6:c.956C>A	ENSP00000371535.2:p.Ser319Tyr
ENST00000503150.1:c.238C>A
ENST00000505513.1:n.256C>A
ENST00000514585.5:c.*657C>A	ENSP00000421880.1:n.*657C>A
NM_016955.3:c.956C>A	NP_058651.3:p.Ser319Tyr
XM_005248168.2:c.719C>A	XP_005248225.1:p.Ser240Tyr
XM_006713965.2:c.776C>A	XP_006714028.1:p.Ser259Tyr
XM_011513846.1:c.953C>A	XP_011512148.1:p.Ser318Tyr
XM_011513847.1:c.923C>A	XP_011512149.1:p.Ser308Tyr
XM_011513848.1:c.776C>A	XP_011512150.1:p.Ser259Tyr
XM_011513846.2:c.953C>A	XP_011512148.1:p.Ser318Tyr
XM_011513847.2:c.923C>A	XP_011512149.1:p.Ser308Tyr
XM_017008277.1:c.1211C>A	XP_016863766.1:p.Ser404Tyr
XM_017008278.1:c.533C>A	XP_016863767.1:p.Ser178Tyr
NM_016955.4:c.956C>A MANE Select	NP_058651.3:p.Ser319Tyr