Canonical Allele Identifier: CA356536881

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146457A>T (hg19) ; chr4:g.25144835A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144835A>T , CM000666.2:g.25144835A>T	GRCh38
NC_000004.11:g.25146457A>T , CM000666.1:g.25146457A>T	GRCh37
NC_000004.10:g.24755555A>T	NCBI36
NG_028222.1:g.20748T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.965T>A MANE Select	ENSP00000371535.2:p.Val322Asp
ENST00000680581.1:c.965T>A	ENSP00000506483.1:p.Val322Asp
ENST00000680824.1:n.2181T>A
ENST00000681071.1:n.1257T>A
ENST00000681341.1:n.2106T>A
ENST00000681948.1:c.1220T>A	ENSP00000505991.1:p.Val407Asp
ENST00000358971.7:c.*763T>A	ENSP00000351857.3:n.*763T>A
ENST00000382103.6:c.965T>A	ENSP00000371535.2:p.Val322Asp
ENST00000503150.1:c.247T>A
ENST00000505513.1:n.265T>A
ENST00000514585.5:c.*666T>A	ENSP00000421880.1:n.*666T>A
NM_016955.3:c.965T>A	NP_058651.3:p.Val322Asp
XM_005248168.2:c.728T>A	XP_005248225.1:p.Val243Asp
XM_006713965.2:c.785T>A	XP_006714028.1:p.Val262Asp
XM_011513846.1:c.962T>A	XP_011512148.1:p.Val321Asp
XM_011513847.1:c.932T>A	XP_011512149.1:p.Val311Asp
XM_011513848.1:c.785T>A	XP_011512150.1:p.Val262Asp
XM_011513846.2:c.962T>A	XP_011512148.1:p.Val321Asp
XM_011513847.2:c.932T>A	XP_011512149.1:p.Val311Asp
XM_017008277.1:c.1220T>A	XP_016863766.1:p.Val407Asp
XM_017008278.1:c.542T>A	XP_016863767.1:p.Val181Asp
NM_016955.4:c.965T>A MANE Select	NP_058651.3:p.Val322Asp