Canonical Allele Identifier: CA356542582

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158502C>A (hg19) ; chr4:g.25156880C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156880C>A , CM000666.2:g.25156880C>A	GRCh38
NC_000004.11:g.25158502C>A , CM000666.1:g.25158502C>A	GRCh37
NC_000004.10:g.24767600C>A	NCBI36
NG_028222.1:g.8703G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.364G>T MANE Select	ENSP00000371535.2:p.Val122Phe
ENST00000680581.1:c.364G>T	ENSP00000506483.1:p.Val122Phe
ENST00000680824.1:n.1580G>T
ENST00000681071.1:n.656G>T
ENST00000681166.1:n.1411G>T
ENST00000681341.1:n.1505G>T
ENST00000681640.1:n.458G>T
ENST00000681948.1:c.619G>T	ENSP00000505991.1:p.Val207Phe
ENST00000358971.7:c.*162G>T	ENSP00000351857.3:n.*162G>T
ENST00000382103.6:c.364G>T	ENSP00000371535.2:p.Val122Phe
ENST00000514585.5:c.*65G>T	ENSP00000421880.1:n.*65G>T
NM_016955.3:c.364G>T	NP_058651.3:p.Val122Phe
XM_005248168.2:c.127G>T	XP_005248225.1:p.Val43Phe
XM_006713965.2:c.184G>T	XP_006714028.1:p.Val62Phe
XM_011513846.1:c.361G>T	XP_011512148.1:p.Val121Phe
XM_011513847.1:c.331G>T	XP_011512149.1:p.Val111Phe
XM_011513848.1:c.184G>T	XP_011512150.1:p.Val62Phe
XM_011513846.2:c.361G>T	XP_011512148.1:p.Val121Phe
XM_011513847.2:c.331G>T	XP_011512149.1:p.Val111Phe
XM_017008277.1:c.619G>T	XP_016863766.1:p.Val207Phe
XM_017008278.1:c.-60G>T	XP_016863767.1:n.-60G>T
NM_016955.4:c.364G>T MANE Select	NP_058651.3:p.Val122Phe