Canonical Allele Identifier: CA356542586

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158503C>G (hg19) ; chr4:g.25156881C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156881C>G , CM000666.2:g.25156881C>G	GRCh38
NC_000004.11:g.25158503C>G , CM000666.1:g.25158503C>G	GRCh37
NC_000004.10:g.24767601C>G	NCBI36
NG_028222.1:g.8702G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.363G>C MANE Select	ENSP00000371535.2:p.Leu121Phe
ENST00000680581.1:c.363G>C	ENSP00000506483.1:p.Leu121Phe
ENST00000680824.1:n.1579G>C
ENST00000681071.1:n.655G>C
ENST00000681166.1:n.1410G>C
ENST00000681341.1:n.1504G>C
ENST00000681640.1:n.457G>C
ENST00000681948.1:c.618G>C	ENSP00000505991.1:p.Leu206Phe
ENST00000358971.7:c.*161G>C	ENSP00000351857.3:n.*161G>C
ENST00000382103.6:c.363G>C	ENSP00000371535.2:p.Leu121Phe
ENST00000514585.5:c.*64G>C	ENSP00000421880.1:n.*64G>C
NM_016955.3:c.363G>C	NP_058651.3:p.Leu121Phe
XM_005248168.2:c.126G>C	XP_005248225.1:p.Leu42Phe
XM_006713965.2:c.183G>C	XP_006714028.1:p.Leu61Phe
XM_011513846.1:c.360G>C	XP_011512148.1:p.Leu120Phe
XM_011513847.1:c.330G>C	XP_011512149.1:p.Leu110Phe
XM_011513848.1:c.183G>C	XP_011512150.1:p.Leu61Phe
XM_011513846.2:c.360G>C	XP_011512148.1:p.Leu120Phe
XM_011513847.2:c.330G>C	XP_011512149.1:p.Leu110Phe
XM_017008277.1:c.618G>C	XP_016863766.1:p.Leu206Phe
XM_017008278.1:c.-61G>C	XP_016863767.1:n.-61G>C
NM_016955.4:c.363G>C MANE Select	NP_058651.3:p.Leu121Phe