Canonical Allele Identifier: CA356542567

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158494G>C (hg19) ; chr4:g.25156872G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156872G>C , CM000666.2:g.25156872G>C	GRCh38
NC_000004.11:g.25158494G>C , CM000666.1:g.25158494G>C	GRCh37
NC_000004.10:g.24767592G>C	NCBI36
NG_028222.1:g.8711C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.372C>G MANE Select	ENSP00000371535.2:p.Asp124Glu
ENST00000680581.1:c.372C>G	ENSP00000506483.1:p.Asp124Glu
ENST00000680824.1:n.1588C>G
ENST00000681071.1:n.664C>G
ENST00000681166.1:n.1419C>G
ENST00000681341.1:n.1513C>G
ENST00000681640.1:n.466C>G
ENST00000681948.1:c.627C>G	ENSP00000505991.1:p.Asp209Glu
ENST00000358971.7:c.*170C>G	ENSP00000351857.3:n.*170C>G
ENST00000382103.6:c.372C>G	ENSP00000371535.2:p.Asp124Glu
ENST00000514585.5:c.*73C>G	ENSP00000421880.1:n.*73C>G
NM_016955.3:c.372C>G	NP_058651.3:p.Asp124Glu
XM_005248168.2:c.135C>G	XP_005248225.1:p.Asp45Glu
XM_006713965.2:c.192C>G	XP_006714028.1:p.Asp64Glu
XM_011513846.1:c.369C>G	XP_011512148.1:p.Asp123Glu
XM_011513847.1:c.339C>G	XP_011512149.1:p.Asp113Glu
XM_011513848.1:c.192C>G	XP_011512150.1:p.Asp64Glu
XM_011513846.2:c.369C>G	XP_011512148.1:p.Asp123Glu
XM_011513847.2:c.339C>G	XP_011512149.1:p.Asp113Glu
XM_017008277.1:c.627C>G	XP_016863766.1:p.Asp209Glu
XM_017008278.1:c.-52C>G	XP_016863767.1:n.-52C>G
NM_016955.4:c.372C>G MANE Select	NP_058651.3:p.Asp124Glu