Canonical Allele Identifier: CA356536639

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146402T>G (hg19) ; chr4:g.25144780T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144780T>G , CM000666.2:g.25144780T>G	GRCh38
NC_000004.11:g.25146402T>G , CM000666.1:g.25146402T>G	GRCh37
NC_000004.10:g.24755500T>G	NCBI36
NG_028222.1:g.20803A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1020A>C MANE Select	ENSP00000371535.2:p.Glu340Asp
ENST00000680581.1:c.1020A>C	ENSP00000506483.1:p.Glu340Asp
ENST00000680824.1:n.2236A>C
ENST00000681071.1:n.1312A>C
ENST00000681341.1:n.2161A>C
ENST00000681948.1:c.1275A>C	ENSP00000505991.1:p.Glu425Asp
ENST00000358971.7:c.*818A>C	ENSP00000351857.3:n.*818A>C
ENST00000382103.6:c.1020A>C	ENSP00000371535.2:p.Glu340Asp
ENST00000503150.1:c.302A>C
ENST00000505513.1:n.320A>C
ENST00000514585.5:c.*721A>C	ENSP00000421880.1:n.*721A>C
NM_016955.3:c.1020A>C	NP_058651.3:p.Glu340Asp
XM_005248168.2:c.783A>C	XP_005248225.1:p.Glu261Asp
XM_006713965.2:c.840A>C	XP_006714028.1:p.Glu280Asp
XM_011513846.1:c.1017A>C	XP_011512148.1:p.Glu339Asp
XM_011513847.1:c.987A>C	XP_011512149.1:p.Glu329Asp
XM_011513848.1:c.840A>C	XP_011512150.1:p.Glu280Asp
XM_011513846.2:c.1017A>C	XP_011512148.1:p.Glu339Asp
XM_011513847.2:c.987A>C	XP_011512149.1:p.Glu329Asp
XM_017008277.1:c.1275A>C	XP_016863766.1:p.Glu425Asp
XM_017008278.1:c.597A>C	XP_016863767.1:p.Glu199Asp
NM_016955.4:c.1020A>C MANE Select	NP_058651.3:p.Glu340Asp