Canonical Allele Identifier: CA356536778

Gene: SEPSECS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.991T>C MANE Select	ENSP00000371535.2:p.Ser331Pro
ENST00000680581.1:c.991T>C	ENSP00000506483.1:p.Ser331Pro
ENST00000680824.1:n.2207T>C
ENST00000681071.1:n.1283T>C
ENST00000681341.1:n.2132T>C
ENST00000681948.1:c.1246T>C	ENSP00000505991.1:p.Ser416Pro
ENST00000358971.7:c.*789T>C	ENSP00000351857.3:n.*789T>C
ENST00000382103.6:c.991T>C	ENSP00000371535.2:p.Ser331Pro
ENST00000503150.1:c.273T>C
ENST00000505513.1:n.291T>C
ENST00000514585.5:c.*692T>C	ENSP00000421880.1:n.*692T>C
NM_016955.3:c.991T>C	NP_058651.3:p.Ser331Pro
XM_005248168.2:c.754T>C	XP_005248225.1:p.Ser252Pro
XM_006713965.2:c.811T>C	XP_006714028.1:p.Ser271Pro
XM_011513846.1:c.988T>C	XP_011512148.1:p.Ser330Pro
XM_011513847.1:c.958T>C	XP_011512149.1:p.Ser320Pro
XM_011513848.1:c.811T>C	XP_011512150.1:p.Ser271Pro
XM_011513846.2:c.988T>C	XP_011512148.1:p.Ser330Pro
XM_011513847.2:c.958T>C	XP_011512149.1:p.Ser320Pro
XM_017008277.1:c.1246T>C	XP_016863766.1:p.Ser416Pro
XM_017008278.1:c.568T>C	XP_016863767.1:p.Ser190Pro
NM_016955.4:c.991T>C MANE Select	NP_058651.3:p.Ser331Pro