Canonical Allele Identifier: CA356536834

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146445A>T (hg19) ; chr4:g.25144823A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144823A>T , CM000666.2:g.25144823A>T	GRCh38
NC_000004.11:g.25146445A>T , CM000666.1:g.25146445A>T	GRCh37
NC_000004.10:g.24755543A>T	NCBI36
NG_028222.1:g.20760T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.977T>A MANE Select	ENSP00000371535.2:p.Leu326Ter
ENST00000680581.1:c.977T>A	ENSP00000506483.1:p.Leu326Ter
ENST00000680824.1:n.2193T>A
ENST00000681071.1:n.1269T>A
ENST00000681341.1:n.2118T>A
ENST00000681948.1:c.1232T>A	ENSP00000505991.1:p.Leu411Ter
ENST00000358971.7:c.*775T>A	ENSP00000351857.3:n.*775T>A
ENST00000382103.6:c.977T>A	ENSP00000371535.2:p.Leu326Ter
ENST00000503150.1:c.259T>A
ENST00000505513.1:n.277T>A
ENST00000514585.5:c.*678T>A	ENSP00000421880.1:n.*678T>A
NM_016955.3:c.977T>A	NP_058651.3:p.Leu326Ter
XM_005248168.2:c.740T>A	XP_005248225.1:p.Leu247Ter
XM_006713965.2:c.797T>A	XP_006714028.1:p.Leu266Ter
XM_011513846.1:c.974T>A	XP_011512148.1:p.Leu325Ter
XM_011513847.1:c.944T>A	XP_011512149.1:p.Leu315Ter
XM_011513848.1:c.797T>A	XP_011512150.1:p.Leu266Ter
XM_011513846.2:c.974T>A	XP_011512148.1:p.Leu325Ter
XM_011513847.2:c.944T>A	XP_011512149.1:p.Leu315Ter
XM_017008277.1:c.1232T>A	XP_016863766.1:p.Leu411Ter
XM_017008278.1:c.554T>A	XP_016863767.1:p.Leu185Ter
NM_016955.4:c.977T>A MANE Select	NP_058651.3:p.Leu326Ter