Canonical Allele Identifier: CA438732719

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158515A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156893A>T , CM000666.2:g.25156893A>T	GRCh38
NC_000004.11:g.25158515A>T , CM000666.1:g.25158515A>T	GRCh37
NC_000004.10:g.24767613A>T	NCBI36
NG_028222.1:g.8690T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.351T>A MANE Select	ENSP00000371535.2:p.Ile117=
ENST00000680581.1:c.351T>A	ENSP00000506483.1:p.Ile117=
ENST00000680824.1:n.1567T>A
ENST00000681071.1:n.643T>A
ENST00000681166.1:n.1398T>A
ENST00000681341.1:n.1492T>A
ENST00000681640.1:n.445T>A
ENST00000681948.1:c.606T>A	ENSP00000505991.1:p.Ile202=
ENST00000358971.7:c.*149T>A	ENSP00000351857.3:n.*149T>A
ENST00000382103.6:c.351T>A	ENSP00000371535.2:p.Ile117=
ENST00000514585.5:c.*52T>A	ENSP00000421880.1:n.*52T>A
NM_016955.3:c.351T>A	NP_058651.3:p.Ile117=
XM_005248168.2:c.114T>A	XP_005248225.1:p.Ile38=
XM_006713965.2:c.171T>A	XP_006714028.1:p.Ile57=
XM_011513846.1:c.348T>A	XP_011512148.1:p.Ile116=
XM_011513847.1:c.318T>A	XP_011512149.1:p.Ile106=
XM_011513848.1:c.171T>A	XP_011512150.1:p.Ile57=
XM_011513846.2:c.348T>A	XP_011512148.1:p.Ile116=
XM_011513847.2:c.318T>A	XP_011512149.1:p.Ile106=
XM_017008277.1:c.606T>A	XP_016863766.1:p.Ile202=
XM_017008278.1:c.-73T>A	XP_016863767.1:n.-73T>A
NM_016955.4:c.351T>A MANE Select	NP_058651.3:p.Ile117=