Canonical Allele Identifier: CA438732337

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146480A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144858A>G , CM000666.2:g.25144858A>G	GRCh38
NC_000004.11:g.25146480A>G , CM000666.1:g.25146480A>G	GRCh37
NC_000004.10:g.24755578A>G	NCBI36
NG_028222.1:g.20725T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.942T>C MANE Select	ENSP00000371535.2:p.Ala314=
ENST00000680581.1:c.942T>C	ENSP00000506483.1:p.Ala314=
ENST00000680824.1:n.2158T>C
ENST00000681071.1:n.1234T>C
ENST00000681341.1:n.2083T>C
ENST00000681948.1:c.1197T>C	ENSP00000505991.1:p.Ala399=
ENST00000358971.7:c.*740T>C	ENSP00000351857.3:n.*740T>C
ENST00000382103.6:c.942T>C	ENSP00000371535.2:p.Ala314=
ENST00000503150.1:c.224T>C
ENST00000505513.1:n.242T>C
ENST00000514585.5:c.*643T>C	ENSP00000421880.1:n.*643T>C
NM_016955.3:c.942T>C	NP_058651.3:p.Ala314=
XM_005248168.2:c.705T>C	XP_005248225.1:p.Ala235=
XM_006713965.2:c.762T>C	XP_006714028.1:p.Ala254=
XM_011513846.1:c.939T>C	XP_011512148.1:p.Ala313=
XM_011513847.1:c.909T>C	XP_011512149.1:p.Ala303=
XM_011513848.1:c.762T>C	XP_011512150.1:p.Ala254=
XM_011513846.2:c.939T>C	XP_011512148.1:p.Ala313=
XM_011513847.2:c.909T>C	XP_011512149.1:p.Ala303=
XM_017008277.1:c.1197T>C	XP_016863766.1:p.Ala399=
XM_017008278.1:c.519T>C	XP_016863767.1:p.Ala173=
NM_016955.4:c.942T>C MANE Select	NP_058651.3:p.Ala314=