Canonical Allele Identifier: CA356536627

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146399T>G (hg19) ; chr4:g.25144777T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144777T>G , CM000666.2:g.25144777T>G	GRCh38
NC_000004.11:g.25146399T>G , CM000666.1:g.25146399T>G	GRCh37
NC_000004.10:g.24755497T>G	NCBI36
NG_028222.1:g.20806A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1023A>C MANE Select	ENSP00000371535.2:p.Arg341Ser
ENST00000680581.1:c.1023A>C	ENSP00000506483.1:p.Arg341Ser
ENST00000680824.1:n.2239A>C
ENST00000681071.1:n.1315A>C
ENST00000681341.1:n.2164A>C
ENST00000681948.1:c.1278A>C	ENSP00000505991.1:p.Arg426Ser
ENST00000358971.7:c.*821A>C	ENSP00000351857.3:n.*821A>C
ENST00000382103.6:c.1023A>C	ENSP00000371535.2:p.Arg341Ser
ENST00000503150.1:c.305A>C
ENST00000505513.1:n.323A>C
ENST00000514585.5:c.*724A>C	ENSP00000421880.1:n.*724A>C
NM_016955.3:c.1023A>C	NP_058651.3:p.Arg341Ser
XM_005248168.2:c.786A>C	XP_005248225.1:p.Arg262Ser
XM_006713965.2:c.843A>C	XP_006714028.1:p.Arg281Ser
XM_011513846.1:c.1020A>C	XP_011512148.1:p.Arg340Ser
XM_011513847.1:c.990A>C	XP_011512149.1:p.Arg330Ser
XM_011513848.1:c.843A>C	XP_011512150.1:p.Arg281Ser
XM_011513846.2:c.1020A>C	XP_011512148.1:p.Arg340Ser
XM_011513847.2:c.990A>C	XP_011512149.1:p.Arg330Ser
XM_017008277.1:c.1278A>C	XP_016863766.1:p.Arg426Ser
XM_017008278.1:c.600A>C	XP_016863767.1:p.Arg200Ser
NM_016955.4:c.1023A>C MANE Select	NP_058651.3:p.Arg341Ser