Canonical Allele Identifier: CA356536938

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146472G>C (hg19) ; chr4:g.25144850G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144850G>C , CM000666.2:g.25144850G>C	GRCh38
NC_000004.11:g.25146472G>C , CM000666.1:g.25146472G>C	GRCh37
NC_000004.10:g.24755570G>C	NCBI36
NG_028222.1:g.20733C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.950C>G MANE Select	ENSP00000371535.2:p.Ser317Ter
ENST00000680581.1:c.950C>G	ENSP00000506483.1:p.Ser317Ter
ENST00000680824.1:n.2166C>G
ENST00000681071.1:n.1242C>G
ENST00000681341.1:n.2091C>G
ENST00000681948.1:c.1205C>G	ENSP00000505991.1:p.Ser402Ter
ENST00000358971.7:c.*748C>G	ENSP00000351857.3:n.*748C>G
ENST00000382103.6:c.950C>G	ENSP00000371535.2:p.Ser317Ter
ENST00000503150.1:c.232C>G
ENST00000505513.1:n.250C>G
ENST00000514585.5:c.*651C>G	ENSP00000421880.1:n.*651C>G
NM_016955.3:c.950C>G	NP_058651.3:p.Ser317Ter
XM_005248168.2:c.713C>G	XP_005248225.1:p.Ser238Ter
XM_006713965.2:c.770C>G	XP_006714028.1:p.Ser257Ter
XM_011513846.1:c.947C>G	XP_011512148.1:p.Ser316Ter
XM_011513847.1:c.917C>G	XP_011512149.1:p.Ser306Ter
XM_011513848.1:c.770C>G	XP_011512150.1:p.Ser257Ter
XM_011513846.2:c.947C>G	XP_011512148.1:p.Ser316Ter
XM_011513847.2:c.917C>G	XP_011512149.1:p.Ser306Ter
XM_017008277.1:c.1205C>G	XP_016863766.1:p.Ser402Ter
XM_017008278.1:c.527C>G	XP_016863767.1:p.Ser176Ter
NM_016955.4:c.950C>G MANE Select	NP_058651.3:p.Ser317Ter