Canonical Allele Identifier: CA438732737

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158539T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156917T>G , CM000666.2:g.25156917T>G	GRCh38
NC_000004.11:g.25158539T>G , CM000666.1:g.25158539T>G	GRCh37
NC_000004.10:g.24767637T>G	NCBI36
NG_028222.1:g.8666A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.327A>C MANE Select	ENSP00000371535.2:p.Ala109=
ENST00000680581.1:c.327A>C	ENSP00000506483.1:p.Ala109=
ENST00000680824.1:n.1543A>C
ENST00000681071.1:n.619A>C
ENST00000681166.1:n.1374A>C
ENST00000681341.1:n.1468A>C
ENST00000681640.1:n.421A>C
ENST00000681948.1:c.582A>C	ENSP00000505991.1:p.Ala194=
ENST00000358971.7:c.*125A>C	ENSP00000351857.3:n.*125A>C
ENST00000382103.6:c.327A>C	ENSP00000371535.2:p.Ala109=
ENST00000514585.5:c.*28A>C	ENSP00000421880.1:n.*28A>C
NM_016955.3:c.327A>C	NP_058651.3:p.Ala109=
XM_005248168.2:c.90A>C	XP_005248225.1:p.Ala30=
XM_006713965.2:c.147A>C	XP_006714028.1:p.Ala49=
XM_011513846.1:c.324A>C	XP_011512148.1:p.Ala108=
XM_011513847.1:c.294A>C	XP_011512149.1:p.Ala98=
XM_011513848.1:c.147A>C	XP_011512150.1:p.Ala49=
XM_011513846.2:c.324A>C	XP_011512148.1:p.Ala108=
XM_011513847.2:c.294A>C	XP_011512149.1:p.Ala98=
XM_017008277.1:c.582A>C	XP_016863766.1:p.Ala194=
XM_017008278.1:c.-97A>C	XP_016863767.1:n.-97A>C
NM_016955.4:c.327A>C MANE Select	NP_058651.3:p.Ala109=