Canonical Allele Identifier: CA356536754

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146425C>G (hg19) ; chr4:g.25144803C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144803C>G , CM000666.2:g.25144803C>G	GRCh38
NC_000004.11:g.25146425C>G , CM000666.1:g.25146425C>G	GRCh37
NC_000004.10:g.24755523C>G	NCBI36
NG_028222.1:g.20780G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.997G>C MANE Select	ENSP00000371535.2:p.Gly333Arg
ENST00000680581.1:c.997G>C	ENSP00000506483.1:p.Gly333Arg
ENST00000680824.1:n.2213G>C
ENST00000681071.1:n.1289G>C
ENST00000681341.1:n.2138G>C
ENST00000681948.1:c.1252G>C	ENSP00000505991.1:p.Gly418Arg
ENST00000358971.7:c.*795G>C	ENSP00000351857.3:n.*795G>C
ENST00000382103.6:c.997G>C	ENSP00000371535.2:p.Gly333Arg
ENST00000503150.1:c.279G>C
ENST00000505513.1:n.297G>C
ENST00000514585.5:c.*698G>C	ENSP00000421880.1:n.*698G>C
NM_016955.3:c.997G>C	NP_058651.3:p.Gly333Arg
XM_005248168.2:c.760G>C	XP_005248225.1:p.Gly254Arg
XM_006713965.2:c.817G>C	XP_006714028.1:p.Gly273Arg
XM_011513846.1:c.994G>C	XP_011512148.1:p.Gly332Arg
XM_011513847.1:c.964G>C	XP_011512149.1:p.Gly322Arg
XM_011513848.1:c.817G>C	XP_011512150.1:p.Gly273Arg
XM_011513846.2:c.994G>C	XP_011512148.1:p.Gly332Arg
XM_011513847.2:c.964G>C	XP_011512149.1:p.Gly322Arg
XM_017008277.1:c.1252G>C	XP_016863766.1:p.Gly418Arg
XM_017008278.1:c.574G>C	XP_016863767.1:p.Gly192Arg
NM_016955.4:c.997G>C MANE Select	NP_058651.3:p.Gly333Arg