Canonical Allele Identifier: CA438732742

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158548T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156926T>A , CM000666.2:g.25156926T>A	GRCh38
NC_000004.11:g.25158548T>A , CM000666.1:g.25158548T>A	GRCh37
NC_000004.10:g.24767646T>A	NCBI36
NG_028222.1:g.8657A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.318A>T MANE Select	ENSP00000371535.2:p.Pro106=
ENST00000680581.1:c.318A>T	ENSP00000506483.1:p.Pro106=
ENST00000680824.1:n.1534A>T
ENST00000681071.1:n.610A>T
ENST00000681166.1:n.1365A>T
ENST00000681341.1:n.1459A>T
ENST00000681640.1:n.412A>T
ENST00000681948.1:c.573A>T	ENSP00000505991.1:p.Pro191=
ENST00000358971.7:c.*116A>T	ENSP00000351857.3:n.*116A>T
ENST00000382103.6:c.318A>T	ENSP00000371535.2:p.Pro106=
ENST00000514585.5:c.*19A>T	ENSP00000421880.1:n.*19A>T
NM_016955.3:c.318A>T	NP_058651.3:p.Pro106=
XM_005248168.2:c.81A>T	XP_005248225.1:p.Pro27=
XM_006713965.2:c.138A>T	XP_006714028.1:p.Pro46=
XM_011513846.1:c.315A>T	XP_011512148.1:p.Pro105=
XM_011513847.1:c.285A>T	XP_011512149.1:p.Pro95=
XM_011513848.1:c.138A>T	XP_011512150.1:p.Pro46=
XM_011513846.2:c.315A>T	XP_011512148.1:p.Pro105=
XM_011513847.2:c.285A>T	XP_011512149.1:p.Pro95=
XM_017008277.1:c.573A>T	XP_016863766.1:p.Pro191=
XM_017008278.1:c.-106A>T	XP_016863767.1:n.-106A>T
NM_016955.4:c.318A>T MANE Select	NP_058651.3:p.Pro106=