Canonical Allele Identifier: CA356542595

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158508A>C (hg19) ; chr4:g.25156886A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156886A>C , CM000666.2:g.25156886A>C	GRCh38
NC_000004.11:g.25158508A>C , CM000666.1:g.25158508A>C	GRCh37
NC_000004.10:g.24767606A>C	NCBI36
NG_028222.1:g.8697T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.358T>G MANE Select	ENSP00000371535.2:p.Ser120Ala
ENST00000680581.1:c.358T>G	ENSP00000506483.1:p.Ser120Ala
ENST00000680824.1:n.1574T>G
ENST00000681071.1:n.650T>G
ENST00000681166.1:n.1405T>G
ENST00000681341.1:n.1499T>G
ENST00000681640.1:n.452T>G
ENST00000681948.1:c.613T>G	ENSP00000505991.1:p.Ser205Ala
ENST00000358971.7:c.*156T>G	ENSP00000351857.3:n.*156T>G
ENST00000382103.6:c.358T>G	ENSP00000371535.2:p.Ser120Ala
ENST00000514585.5:c.*59T>G	ENSP00000421880.1:n.*59T>G
NM_016955.3:c.358T>G	NP_058651.3:p.Ser120Ala
XM_005248168.2:c.121T>G	XP_005248225.1:p.Ser41Ala
XM_006713965.2:c.178T>G	XP_006714028.1:p.Ser60Ala
XM_011513846.1:c.355T>G	XP_011512148.1:p.Ser119Ala
XM_011513847.1:c.325T>G	XP_011512149.1:p.Ser109Ala
XM_011513848.1:c.178T>G	XP_011512150.1:p.Ser60Ala
XM_011513846.2:c.355T>G	XP_011512148.1:p.Ser119Ala
XM_011513847.2:c.325T>G	XP_011512149.1:p.Ser109Ala
XM_017008277.1:c.613T>G	XP_016863766.1:p.Ser205Ala
XM_017008278.1:c.-66T>G	XP_016863767.1:n.-66T>G
NM_016955.4:c.358T>G MANE Select	NP_058651.3:p.Ser120Ala