Canonical Allele Identifier: CA356542693

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158535A>C (hg19) ; chr4:g.25156913A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156913A>C , CM000666.2:g.25156913A>C	GRCh38
NC_000004.11:g.25158535A>C , CM000666.1:g.25158535A>C	GRCh37
NC_000004.10:g.24767633A>C	NCBI36
NG_028222.1:g.8670T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.331T>G MANE Select	ENSP00000371535.2:p.Ser111Ala
ENST00000680581.1:c.331T>G	ENSP00000506483.1:p.Ser111Ala
ENST00000680824.1:n.1547T>G
ENST00000681071.1:n.623T>G
ENST00000681166.1:n.1378T>G
ENST00000681341.1:n.1472T>G
ENST00000681640.1:n.425T>G
ENST00000681948.1:c.586T>G	ENSP00000505991.1:p.Ser196Ala
ENST00000358971.7:c.*129T>G	ENSP00000351857.3:n.*129T>G
ENST00000382103.6:c.331T>G	ENSP00000371535.2:p.Ser111Ala
ENST00000514585.5:c.*32T>G	ENSP00000421880.1:n.*32T>G
NM_016955.3:c.331T>G	NP_058651.3:p.Ser111Ala
XM_005248168.2:c.94T>G	XP_005248225.1:p.Ser32Ala
XM_006713965.2:c.151T>G	XP_006714028.1:p.Ser51Ala
XM_011513846.1:c.328T>G	XP_011512148.1:p.Ser110Ala
XM_011513847.1:c.298T>G	XP_011512149.1:p.Ser100Ala
XM_011513848.1:c.151T>G	XP_011512150.1:p.Ser51Ala
XM_011513846.2:c.328T>G	XP_011512148.1:p.Ser110Ala
XM_011513847.2:c.298T>G	XP_011512149.1:p.Ser100Ala
XM_017008277.1:c.586T>G	XP_016863766.1:p.Ser196Ala
XM_017008278.1:c.-93T>G	XP_016863767.1:n.-93T>G
NM_016955.4:c.331T>G MANE Select	NP_058651.3:p.Ser111Ala