Canonical Allele Identifier: CA438732709

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158500G>C (hg19)

Genomic Alleles

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

Transcript Alleles

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