Canonical Allele Identifier: CA438732710

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156878-G-T
• MyVariant Identifiers: chr4:g.25158500G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156878G>T , CM000666.2:g.25156878G>T	GRCh38
NC_000004.11:g.25158500G>T , CM000666.1:g.25158500G>T	GRCh37
NC_000004.10:g.24767598G>T	NCBI36
NG_028222.1:g.8705C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.366C>A MANE Select	ENSP00000371535.2:p.Val122=
ENST00000680581.1:c.366C>A	ENSP00000506483.1:p.Val122=
ENST00000680824.1:n.1582C>A
ENST00000681071.1:n.658C>A
ENST00000681166.1:n.1413C>A
ENST00000681341.1:n.1507C>A
ENST00000681640.1:n.460C>A
ENST00000681948.1:c.621C>A	ENSP00000505991.1:p.Val207=
ENST00000358971.7:c.*164C>A	ENSP00000351857.3:n.*164C>A
ENST00000382103.6:c.366C>A	ENSP00000371535.2:p.Val122=
ENST00000514585.5:c.*67C>A	ENSP00000421880.1:n.*67C>A
NM_016955.3:c.366C>A	NP_058651.3:p.Val122=
XM_005248168.2:c.129C>A	XP_005248225.1:p.Val43=
XM_006713965.2:c.186C>A	XP_006714028.1:p.Val62=
XM_011513846.1:c.363C>A	XP_011512148.1:p.Val121=
XM_011513847.1:c.333C>A	XP_011512149.1:p.Val111=
XM_011513848.1:c.186C>A	XP_011512150.1:p.Val62=
XM_011513846.2:c.363C>A	XP_011512148.1:p.Val121=
XM_011513847.2:c.333C>A	XP_011512149.1:p.Val111=
XM_017008277.1:c.621C>A	XP_016863766.1:p.Val207=
XM_017008278.1:c.-58C>A	XP_016863767.1:n.-58C>A
NM_016955.4:c.366C>A MANE Select	NP_058651.3:p.Val122=