Canonical Allele Identifier: CA356536776

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146431A>C (hg19) ; chr4:g.25144809A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144809A>C , CM000666.2:g.25144809A>C	GRCh38
NC_000004.11:g.25146431A>C , CM000666.1:g.25146431A>C	GRCh37
NC_000004.10:g.24755529A>C	NCBI36
NG_028222.1:g.20774T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.991T>G MANE Select	ENSP00000371535.2:p.Ser331Ala
ENST00000680581.1:c.991T>G	ENSP00000506483.1:p.Ser331Ala
ENST00000680824.1:n.2207T>G
ENST00000681071.1:n.1283T>G
ENST00000681341.1:n.2132T>G
ENST00000681948.1:c.1246T>G	ENSP00000505991.1:p.Ser416Ala
ENST00000358971.7:c.*789T>G	ENSP00000351857.3:n.*789T>G
ENST00000382103.6:c.991T>G	ENSP00000371535.2:p.Ser331Ala
ENST00000503150.1:c.273T>G
ENST00000505513.1:n.291T>G
ENST00000514585.5:c.*692T>G	ENSP00000421880.1:n.*692T>G
NM_016955.3:c.991T>G	NP_058651.3:p.Ser331Ala
XM_005248168.2:c.754T>G	XP_005248225.1:p.Ser252Ala
XM_006713965.2:c.811T>G	XP_006714028.1:p.Ser271Ala
XM_011513846.1:c.988T>G	XP_011512148.1:p.Ser330Ala
XM_011513847.1:c.958T>G	XP_011512149.1:p.Ser320Ala
XM_011513848.1:c.811T>G	XP_011512150.1:p.Ser271Ala
XM_011513846.2:c.988T>G	XP_011512148.1:p.Ser330Ala
XM_011513847.2:c.958T>G	XP_011512149.1:p.Ser320Ala
XM_017008277.1:c.1246T>G	XP_016863766.1:p.Ser416Ala
XM_017008278.1:c.568T>G	XP_016863767.1:p.Ser190Ala
NM_016955.4:c.991T>G MANE Select	NP_058651.3:p.Ser331Ala