Canonical Allele Identifier: CA356536918

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146467A>C (hg19) ; chr4:g.25144845A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144845A>C , CM000666.2:g.25144845A>C	GRCh38
NC_000004.11:g.25146467A>C , CM000666.1:g.25146467A>C	GRCh37
NC_000004.10:g.24755565A>C	NCBI36
NG_028222.1:g.20738T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.955T>G MANE Select	ENSP00000371535.2:p.Ser319Ala
ENST00000680581.1:c.955T>G	ENSP00000506483.1:p.Ser319Ala
ENST00000680824.1:n.2171T>G
ENST00000681071.1:n.1247T>G
ENST00000681341.1:n.2096T>G
ENST00000681948.1:c.1210T>G	ENSP00000505991.1:p.Ser404Ala
ENST00000358971.7:c.*753T>G	ENSP00000351857.3:n.*753T>G
ENST00000382103.6:c.955T>G	ENSP00000371535.2:p.Ser319Ala
ENST00000503150.1:c.237T>G
ENST00000505513.1:n.255T>G
ENST00000514585.5:c.*656T>G	ENSP00000421880.1:n.*656T>G
NM_016955.3:c.955T>G	NP_058651.3:p.Ser319Ala
XM_005248168.2:c.718T>G	XP_005248225.1:p.Ser240Ala
XM_006713965.2:c.775T>G	XP_006714028.1:p.Ser259Ala
XM_011513846.1:c.952T>G	XP_011512148.1:p.Ser318Ala
XM_011513847.1:c.922T>G	XP_011512149.1:p.Ser308Ala
XM_011513848.1:c.775T>G	XP_011512150.1:p.Ser259Ala
XM_011513846.2:c.952T>G	XP_011512148.1:p.Ser318Ala
XM_011513847.2:c.922T>G	XP_011512149.1:p.Ser308Ala
XM_017008277.1:c.1210T>G	XP_016863766.1:p.Ser404Ala
XM_017008278.1:c.532T>G	XP_016863767.1:p.Ser178Ala
NM_016955.4:c.955T>G MANE Select	NP_058651.3:p.Ser319Ala