Canonical Allele Identifier: CA356542569

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158495T>A (hg19) ; chr4:g.25156873T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156873T>A , CM000666.2:g.25156873T>A	GRCh38
NC_000004.11:g.25158495T>A , CM000666.1:g.25158495T>A	GRCh37
NC_000004.10:g.24767593T>A	NCBI36
NG_028222.1:g.8710A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.371A>T MANE Select	ENSP00000371535.2:p.Asp124Val
ENST00000680581.1:c.371A>T	ENSP00000506483.1:p.Asp124Val
ENST00000680824.1:n.1587A>T
ENST00000681071.1:n.663A>T
ENST00000681166.1:n.1418A>T
ENST00000681341.1:n.1512A>T
ENST00000681640.1:n.465A>T
ENST00000681948.1:c.626A>T	ENSP00000505991.1:p.Asp209Val
ENST00000358971.7:c.*169A>T	ENSP00000351857.3:n.*169A>T
ENST00000382103.6:c.371A>T	ENSP00000371535.2:p.Asp124Val
ENST00000514585.5:c.*72A>T	ENSP00000421880.1:n.*72A>T
NM_016955.3:c.371A>T	NP_058651.3:p.Asp124Val
XM_005248168.2:c.134A>T	XP_005248225.1:p.Asp45Val
XM_006713965.2:c.191A>T	XP_006714028.1:p.Asp64Val
XM_011513846.1:c.368A>T	XP_011512148.1:p.Asp123Val
XM_011513847.1:c.338A>T	XP_011512149.1:p.Asp113Val
XM_011513848.1:c.191A>T	XP_011512150.1:p.Asp64Val
XM_011513846.2:c.368A>T	XP_011512148.1:p.Asp123Val
XM_011513847.2:c.338A>T	XP_011512149.1:p.Asp113Val
XM_017008277.1:c.626A>T	XP_016863766.1:p.Asp209Val
XM_017008278.1:c.-53A>T	XP_016863767.1:n.-53A>T
NM_016955.4:c.371A>T MANE Select	NP_058651.3:p.Asp124Val