Canonical Allele Identifier: CA356536846

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146449T>A (hg19) ; chr4:g.25144827T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144827T>A , CM000666.2:g.25144827T>A	GRCh38
NC_000004.11:g.25146449T>A , CM000666.1:g.25146449T>A	GRCh37
NC_000004.10:g.24755547T>A	NCBI36
NG_028222.1:g.20756A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.973A>T MANE Select	ENSP00000371535.2:p.Thr325Ser
ENST00000680581.1:c.973A>T	ENSP00000506483.1:p.Thr325Ser
ENST00000680824.1:n.2189A>T
ENST00000681071.1:n.1265A>T
ENST00000681341.1:n.2114A>T
ENST00000681948.1:c.1228A>T	ENSP00000505991.1:p.Thr410Ser
ENST00000358971.7:c.*771A>T	ENSP00000351857.3:n.*771A>T
ENST00000382103.6:c.973A>T	ENSP00000371535.2:p.Thr325Ser
ENST00000503150.1:c.255A>T
ENST00000505513.1:n.273A>T
ENST00000514585.5:c.*674A>T	ENSP00000421880.1:n.*674A>T
NM_016955.3:c.973A>T	NP_058651.3:p.Thr325Ser
XM_005248168.2:c.736A>T	XP_005248225.1:p.Thr246Ser
XM_006713965.2:c.793A>T	XP_006714028.1:p.Thr265Ser
XM_011513846.1:c.970A>T	XP_011512148.1:p.Thr324Ser
XM_011513847.1:c.940A>T	XP_011512149.1:p.Thr314Ser
XM_011513848.1:c.793A>T	XP_011512150.1:p.Thr265Ser
XM_011513846.2:c.970A>T	XP_011512148.1:p.Thr324Ser
XM_011513847.2:c.940A>T	XP_011512149.1:p.Thr314Ser
XM_017008277.1:c.1228A>T	XP_016863766.1:p.Thr410Ser
XM_017008278.1:c.550A>T	XP_016863767.1:p.Thr184Ser
NM_016955.4:c.973A>T MANE Select	NP_058651.3:p.Thr325Ser