Canonical Allele Identifier: CA438732705

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158497C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156875C>A , CM000666.2:g.25156875C>A	GRCh38
NC_000004.11:g.25158497C>A , CM000666.1:g.25158497C>A	GRCh37
NC_000004.10:g.24767595C>A	NCBI36
NG_028222.1:g.8708G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.369G>T MANE Select	ENSP00000371535.2:p.Leu123=
ENST00000680581.1:c.369G>T	ENSP00000506483.1:p.Leu123=
ENST00000680824.1:n.1585G>T
ENST00000681071.1:n.661G>T
ENST00000681166.1:n.1416G>T
ENST00000681341.1:n.1510G>T
ENST00000681640.1:n.463G>T
ENST00000681948.1:c.624G>T	ENSP00000505991.1:p.Leu208=
ENST00000358971.7:c.*167G>T	ENSP00000351857.3:n.*167G>T
ENST00000382103.6:c.369G>T	ENSP00000371535.2:p.Leu123=
ENST00000514585.5:c.*70G>T	ENSP00000421880.1:n.*70G>T
NM_016955.3:c.369G>T	NP_058651.3:p.Leu123=
XM_005248168.2:c.132G>T	XP_005248225.1:p.Leu44=
XM_006713965.2:c.189G>T	XP_006714028.1:p.Leu63=
XM_011513846.1:c.366G>T	XP_011512148.1:p.Leu122=
XM_011513847.1:c.336G>T	XP_011512149.1:p.Leu112=
XM_011513848.1:c.189G>T	XP_011512150.1:p.Leu63=
XM_011513846.2:c.366G>T	XP_011512148.1:p.Leu122=
XM_011513847.2:c.336G>T	XP_011512149.1:p.Leu112=
XM_017008277.1:c.624G>T	XP_016863766.1:p.Leu208=
XM_017008278.1:c.-55G>T	XP_016863767.1:n.-55G>T
NM_016955.4:c.369G>T MANE Select	NP_058651.3:p.Leu123=