Canonical Allele Identifier: CA438732292

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146426A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144804A>G , CM000666.2:g.25144804A>G	GRCh38
NC_000004.11:g.25146426A>G , CM000666.1:g.25146426A>G	GRCh37
NC_000004.10:g.24755524A>G	NCBI36
NG_028222.1:g.20779T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.996T>C MANE Select	ENSP00000371535.2:p.Asn332=
ENST00000680581.1:c.996T>C	ENSP00000506483.1:p.Asn332=
ENST00000680824.1:n.2212T>C
ENST00000681071.1:n.1288T>C
ENST00000681341.1:n.2137T>C
ENST00000681948.1:c.1251T>C	ENSP00000505991.1:p.Asn417=
ENST00000358971.7:c.*794T>C	ENSP00000351857.3:n.*794T>C
ENST00000382103.6:c.996T>C	ENSP00000371535.2:p.Asn332=
ENST00000503150.1:c.278T>C
ENST00000505513.1:n.296T>C
ENST00000514585.5:c.*697T>C	ENSP00000421880.1:n.*697T>C
NM_016955.3:c.996T>C	NP_058651.3:p.Asn332=
XM_005248168.2:c.759T>C	XP_005248225.1:p.Asn253=
XM_006713965.2:c.816T>C	XP_006714028.1:p.Asn272=
XM_011513846.1:c.993T>C	XP_011512148.1:p.Asn331=
XM_011513847.1:c.963T>C	XP_011512149.1:p.Asn321=
XM_011513848.1:c.816T>C	XP_011512150.1:p.Asn272=
XM_011513846.2:c.993T>C	XP_011512148.1:p.Asn331=
XM_011513847.2:c.963T>C	XP_011512149.1:p.Asn321=
XM_017008277.1:c.1251T>C	XP_016863766.1:p.Asn417=
XM_017008278.1:c.573T>C	XP_016863767.1:p.Asn191=
NM_016955.4:c.996T>C MANE Select	NP_058651.3:p.Asn332=