Canonical Allele Identifier: CA356536832

Gene: SEPSECS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.977T>C MANE Select	ENSP00000371535.2:p.Leu326Ser
ENST00000680581.1:c.977T>C	ENSP00000506483.1:p.Leu326Ser
ENST00000680824.1:n.2193T>C
ENST00000681071.1:n.1269T>C
ENST00000681341.1:n.2118T>C
ENST00000681948.1:c.1232T>C	ENSP00000505991.1:p.Leu411Ser
ENST00000358971.7:c.*775T>C	ENSP00000351857.3:n.*775T>C
ENST00000382103.6:c.977T>C	ENSP00000371535.2:p.Leu326Ser
ENST00000503150.1:c.259T>C
ENST00000505513.1:n.277T>C
ENST00000514585.5:c.*678T>C	ENSP00000421880.1:n.*678T>C
NM_016955.3:c.977T>C	NP_058651.3:p.Leu326Ser
XM_005248168.2:c.740T>C	XP_005248225.1:p.Leu247Ser
XM_006713965.2:c.797T>C	XP_006714028.1:p.Leu266Ser
XM_011513846.1:c.974T>C	XP_011512148.1:p.Leu325Ser
XM_011513847.1:c.944T>C	XP_011512149.1:p.Leu315Ser
XM_011513848.1:c.797T>C	XP_011512150.1:p.Leu266Ser
XM_011513846.2:c.974T>C	XP_011512148.1:p.Leu325Ser
XM_011513847.2:c.944T>C	XP_011512149.1:p.Leu315Ser
XM_017008277.1:c.1232T>C	XP_016863766.1:p.Leu411Ser
XM_017008278.1:c.554T>C	XP_016863767.1:p.Leu185Ser
NM_016955.4:c.977T>C MANE Select	NP_058651.3:p.Leu326Ser