Canonical Allele Identifier: CA438732327

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146471T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144849T>A , CM000666.2:g.25144849T>A	GRCh38
NC_000004.11:g.25146471T>A , CM000666.1:g.25146471T>A	GRCh37
NC_000004.10:g.24755569T>A	NCBI36
NG_028222.1:g.20734A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.951A>T MANE Select	ENSP00000371535.2:p.Ser317=
ENST00000680581.1:c.951A>T	ENSP00000506483.1:p.Ser317=
ENST00000680824.1:n.2167A>T
ENST00000681071.1:n.1243A>T
ENST00000681341.1:n.2092A>T
ENST00000681948.1:c.1206A>T	ENSP00000505991.1:p.Ser402=
ENST00000358971.7:c.*749A>T	ENSP00000351857.3:n.*749A>T
ENST00000382103.6:c.951A>T	ENSP00000371535.2:p.Ser317=
ENST00000503150.1:c.233A>T
ENST00000505513.1:n.251A>T
ENST00000514585.5:c.*652A>T	ENSP00000421880.1:n.*652A>T
NM_016955.3:c.951A>T	NP_058651.3:p.Ser317=
XM_005248168.2:c.714A>T	XP_005248225.1:p.Ser238=
XM_006713965.2:c.771A>T	XP_006714028.1:p.Ser257=
XM_011513846.1:c.948A>T	XP_011512148.1:p.Ser316=
XM_011513847.1:c.918A>T	XP_011512149.1:p.Ser306=
XM_011513848.1:c.771A>T	XP_011512150.1:p.Ser257=
XM_011513846.2:c.948A>T	XP_011512148.1:p.Ser316=
XM_011513847.2:c.918A>T	XP_011512149.1:p.Ser306=
XM_017008277.1:c.1206A>T	XP_016863766.1:p.Ser402=
XM_017008278.1:c.528A>T	XP_016863767.1:p.Ser176=
NM_016955.4:c.951A>T MANE Select	NP_058651.3:p.Ser317=