Canonical Allele Identifier: CA356536633

Gene: SEPSECS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1021A>T MANE Select	ENSP00000371535.2:p.Arg341Ter
ENST00000680581.1:c.1021A>T	ENSP00000506483.1:p.Arg341Ter
ENST00000680824.1:n.2237A>T
ENST00000681071.1:n.1313A>T
ENST00000681341.1:n.2162A>T
ENST00000681948.1:c.1276A>T	ENSP00000505991.1:p.Arg426Ter
ENST00000358971.7:c.*819A>T	ENSP00000351857.3:n.*819A>T
ENST00000382103.6:c.1021A>T	ENSP00000371535.2:p.Arg341Ter
ENST00000503150.1:c.303A>T
ENST00000505513.1:n.321A>T
ENST00000514585.5:c.*722A>T	ENSP00000421880.1:n.*722A>T
NM_016955.3:c.1021A>T	NP_058651.3:p.Arg341Ter
XM_005248168.2:c.784A>T	XP_005248225.1:p.Arg262Ter
XM_006713965.2:c.841A>T	XP_006714028.1:p.Arg281Ter
XM_011513846.1:c.1018A>T	XP_011512148.1:p.Arg340Ter
XM_011513847.1:c.988A>T	XP_011512149.1:p.Arg330Ter
XM_011513848.1:c.841A>T	XP_011512150.1:p.Arg281Ter
XM_011513846.2:c.1018A>T	XP_011512148.1:p.Arg340Ter
XM_011513847.2:c.988A>T	XP_011512149.1:p.Arg330Ter
XM_017008277.1:c.1276A>T	XP_016863766.1:p.Arg426Ter
XM_017008278.1:c.598A>T	XP_016863767.1:p.Arg200Ter
NM_016955.4:c.1021A>T MANE Select	NP_058651.3:p.Arg341Ter