Canonical Allele Identifier: CA356536635

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146401T>C (hg19) ; chr4:g.25144779T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144779T>C , CM000666.2:g.25144779T>C	GRCh38
NC_000004.11:g.25146401T>C , CM000666.1:g.25146401T>C	GRCh37
NC_000004.10:g.24755499T>C	NCBI36
NG_028222.1:g.20804A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1021A>G MANE Select	ENSP00000371535.2:p.Arg341Gly
ENST00000680581.1:c.1021A>G	ENSP00000506483.1:p.Arg341Gly
ENST00000680824.1:n.2237A>G
ENST00000681071.1:n.1313A>G
ENST00000681341.1:n.2162A>G
ENST00000681948.1:c.1276A>G	ENSP00000505991.1:p.Arg426Gly
ENST00000358971.7:c.*819A>G	ENSP00000351857.3:n.*819A>G
ENST00000382103.6:c.1021A>G	ENSP00000371535.2:p.Arg341Gly
ENST00000503150.1:c.303A>G
ENST00000505513.1:n.321A>G
ENST00000514585.5:c.*722A>G	ENSP00000421880.1:n.*722A>G
NM_016955.3:c.1021A>G	NP_058651.3:p.Arg341Gly
XM_005248168.2:c.784A>G	XP_005248225.1:p.Arg262Gly
XM_006713965.2:c.841A>G	XP_006714028.1:p.Arg281Gly
XM_011513846.1:c.1018A>G	XP_011512148.1:p.Arg340Gly
XM_011513847.1:c.988A>G	XP_011512149.1:p.Arg330Gly
XM_011513848.1:c.841A>G	XP_011512150.1:p.Arg281Gly
XM_011513846.2:c.1018A>G	XP_011512148.1:p.Arg340Gly
XM_011513847.2:c.988A>G	XP_011512149.1:p.Arg330Gly
XM_017008277.1:c.1276A>G	XP_016863766.1:p.Arg426Gly
XM_017008278.1:c.598A>G	XP_016863767.1:p.Arg200Gly
NM_016955.4:c.1021A>G MANE Select	NP_058651.3:p.Arg341Gly