Canonical Allele Identifier: CA356536942

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146473A>T (hg19) ; chr4:g.25144851A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144851A>T , CM000666.2:g.25144851A>T	GRCh38
NC_000004.11:g.25146473A>T , CM000666.1:g.25146473A>T	GRCh37
NC_000004.10:g.24755571A>T	NCBI36
NG_028222.1:g.20732T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.949T>A MANE Select	ENSP00000371535.2:p.Ser317Thr
ENST00000680581.1:c.949T>A	ENSP00000506483.1:p.Ser317Thr
ENST00000680824.1:n.2165T>A
ENST00000681071.1:n.1241T>A
ENST00000681341.1:n.2090T>A
ENST00000681948.1:c.1204T>A	ENSP00000505991.1:p.Ser402Thr
ENST00000358971.7:c.*747T>A	ENSP00000351857.3:n.*747T>A
ENST00000382103.6:c.949T>A	ENSP00000371535.2:p.Ser317Thr
ENST00000503150.1:c.231T>A
ENST00000505513.1:n.249T>A
ENST00000514585.5:c.*650T>A	ENSP00000421880.1:n.*650T>A
NM_016955.3:c.949T>A	NP_058651.3:p.Ser317Thr
XM_005248168.2:c.712T>A	XP_005248225.1:p.Ser238Thr
XM_006713965.2:c.769T>A	XP_006714028.1:p.Ser257Thr
XM_011513846.1:c.946T>A	XP_011512148.1:p.Ser316Thr
XM_011513847.1:c.916T>A	XP_011512149.1:p.Ser306Thr
XM_011513848.1:c.769T>A	XP_011512150.1:p.Ser257Thr
XM_011513846.2:c.946T>A	XP_011512148.1:p.Ser316Thr
XM_011513847.2:c.916T>A	XP_011512149.1:p.Ser306Thr
XM_017008277.1:c.1204T>A	XP_016863766.1:p.Ser402Thr
XM_017008278.1:c.526T>A	XP_016863767.1:p.Ser176Thr
NM_016955.4:c.949T>A MANE Select	NP_058651.3:p.Ser317Thr