Canonical Allele Identifier: CA438732699

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156863-C-T
• MyVariant Identifiers: chr4:g.25158485C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156863C>T , CM000666.2:g.25156863C>T	GRCh38
NC_000004.11:g.25158485C>T , CM000666.1:g.25158485C>T	GRCh37
NC_000004.10:g.24767583C>T	NCBI36
NG_028222.1:g.8720G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.381G>A MANE Select	ENSP00000371535.2:p.Lys127=
ENST00000680581.1:c.381G>A	ENSP00000506483.1:p.Lys127=
ENST00000680824.1:n.1597G>A
ENST00000681071.1:n.673G>A
ENST00000681166.1:n.1428G>A
ENST00000681341.1:n.1522G>A
ENST00000681640.1:n.475G>A
ENST00000681948.1:c.636G>A	ENSP00000505991.1:p.Lys212=
ENST00000358971.7:c.*179G>A	ENSP00000351857.3:n.*179G>A
ENST00000382103.6:c.381G>A	ENSP00000371535.2:p.Lys127=
ENST00000514585.5:c.*82G>A	ENSP00000421880.1:n.*82G>A
NM_016955.3:c.381G>A	NP_058651.3:p.Lys127=
XM_005248168.2:c.144G>A	XP_005248225.1:p.Lys48=
XM_006713965.2:c.201G>A	XP_006714028.1:p.Lys67=
XM_011513846.1:c.378G>A	XP_011512148.1:p.Lys126=
XM_011513847.1:c.348G>A	XP_011512149.1:p.Lys116=
XM_011513848.1:c.201G>A	XP_011512150.1:p.Lys67=
XM_011513846.2:c.378G>A	XP_011512148.1:p.Lys126=
XM_011513847.2:c.348G>A	XP_011512149.1:p.Lys116=
XM_017008277.1:c.636G>A	XP_016863766.1:p.Lys212=
XM_017008278.1:c.-43G>A	XP_016863767.1:n.-43G>A
NM_016955.4:c.381G>A MANE Select	NP_058651.3:p.Lys127=