Canonical Allele Identifier: CA356536887

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146458C>T (hg19) ; chr4:g.25144836C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144836C>T , CM000666.2:g.25144836C>T	GRCh38
NC_000004.11:g.25146458C>T , CM000666.1:g.25146458C>T	GRCh37
NC_000004.10:g.24755556C>T	NCBI36
NG_028222.1:g.20747G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.964G>A MANE Select	ENSP00000371535.2:p.Val322Ile
ENST00000680581.1:c.964G>A	ENSP00000506483.1:p.Val322Ile
ENST00000680824.1:n.2180G>A
ENST00000681071.1:n.1256G>A
ENST00000681341.1:n.2105G>A
ENST00000681948.1:c.1219G>A	ENSP00000505991.1:p.Val407Ile
ENST00000358971.7:c.*762G>A	ENSP00000351857.3:n.*762G>A
ENST00000382103.6:c.964G>A	ENSP00000371535.2:p.Val322Ile
ENST00000503150.1:c.246G>A
ENST00000505513.1:n.264G>A
ENST00000514585.5:c.*665G>A	ENSP00000421880.1:n.*665G>A
NM_016955.3:c.964G>A	NP_058651.3:p.Val322Ile
XM_005248168.2:c.727G>A	XP_005248225.1:p.Val243Ile
XM_006713965.2:c.784G>A	XP_006714028.1:p.Val262Ile
XM_011513846.1:c.961G>A	XP_011512148.1:p.Val321Ile
XM_011513847.1:c.931G>A	XP_011512149.1:p.Val311Ile
XM_011513848.1:c.784G>A	XP_011512150.1:p.Val262Ile
XM_011513846.2:c.961G>A	XP_011512148.1:p.Val321Ile
XM_011513847.2:c.931G>A	XP_011512149.1:p.Val311Ile
XM_017008277.1:c.1219G>A	XP_016863766.1:p.Val407Ile
XM_017008278.1:c.541G>A	XP_016863767.1:p.Val181Ile
NM_016955.4:c.964G>A MANE Select	NP_058651.3:p.Val322Ile