Canonical Allele Identifier: CA356536956

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146476C>T (hg19) ; chr4:g.25144854C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144854C>T , CM000666.2:g.25144854C>T	GRCh38
NC_000004.11:g.25146476C>T , CM000666.1:g.25146476C>T	GRCh37
NC_000004.10:g.24755574C>T	NCBI36
NG_028222.1:g.20729G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.946G>A MANE Select	ENSP00000371535.2:p.Ala316Thr
ENST00000680581.1:c.946G>A	ENSP00000506483.1:p.Ala316Thr
ENST00000680824.1:n.2162G>A
ENST00000681071.1:n.1238G>A
ENST00000681341.1:n.2087G>A
ENST00000681948.1:c.1201G>A	ENSP00000505991.1:p.Ala401Thr
ENST00000358971.7:c.*744G>A	ENSP00000351857.3:n.*744G>A
ENST00000382103.6:c.946G>A	ENSP00000371535.2:p.Ala316Thr
ENST00000503150.1:c.228G>A
ENST00000505513.1:n.246G>A
ENST00000514585.5:c.*647G>A	ENSP00000421880.1:n.*647G>A
NM_016955.3:c.946G>A	NP_058651.3:p.Ala316Thr
XM_005248168.2:c.709G>A	XP_005248225.1:p.Ala237Thr
XM_006713965.2:c.766G>A	XP_006714028.1:p.Ala256Thr
XM_011513846.1:c.943G>A	XP_011512148.1:p.Ala315Thr
XM_011513847.1:c.913G>A	XP_011512149.1:p.Ala305Thr
XM_011513848.1:c.766G>A	XP_011512150.1:p.Ala256Thr
XM_011513846.2:c.943G>A	XP_011512148.1:p.Ala315Thr
XM_011513847.2:c.913G>A	XP_011512149.1:p.Ala305Thr
XM_017008277.1:c.1201G>A	XP_016863766.1:p.Ala401Thr
XM_017008278.1:c.523G>A	XP_016863767.1:p.Ala175Thr
NM_016955.4:c.946G>A MANE Select	NP_058651.3:p.Ala316Thr