Canonical Allele Identifier: CA356536752

Gene: SEPSECS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.997G>T MANE Select	ENSP00000371535.2:p.Gly333Cys
ENST00000680581.1:c.997G>T	ENSP00000506483.1:p.Gly333Cys
ENST00000680824.1:n.2213G>T
ENST00000681071.1:n.1289G>T
ENST00000681341.1:n.2138G>T
ENST00000681948.1:c.1252G>T	ENSP00000505991.1:p.Gly418Cys
ENST00000358971.7:c.*795G>T	ENSP00000351857.3:n.*795G>T
ENST00000382103.6:c.997G>T	ENSP00000371535.2:p.Gly333Cys
ENST00000503150.1:c.279G>T
ENST00000505513.1:n.297G>T
ENST00000514585.5:c.*698G>T	ENSP00000421880.1:n.*698G>T
NM_016955.3:c.997G>T	NP_058651.3:p.Gly333Cys
XM_005248168.2:c.760G>T	XP_005248225.1:p.Gly254Cys
XM_006713965.2:c.817G>T	XP_006714028.1:p.Gly273Cys
XM_011513846.1:c.994G>T	XP_011512148.1:p.Gly332Cys
XM_011513847.1:c.964G>T	XP_011512149.1:p.Gly322Cys
XM_011513848.1:c.817G>T	XP_011512150.1:p.Gly273Cys
XM_011513846.2:c.994G>T	XP_011512148.1:p.Gly332Cys
XM_011513847.2:c.964G>T	XP_011512149.1:p.Gly322Cys
XM_017008277.1:c.1252G>T	XP_016863766.1:p.Gly418Cys
XM_017008278.1:c.574G>T	XP_016863767.1:p.Gly192Cys
NM_016955.4:c.997G>T MANE Select	NP_058651.3:p.Gly333Cys