Canonical Allele Identifier: CA356542570

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156873-T-C
• MyVariant Identifiers: chr4:g.25158495T>C (hg19) ; chr4:g.25156873T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.371A>G MANE Select	ENSP00000371535.2:p.Asp124Gly
ENST00000680581.1:c.371A>G	ENSP00000506483.1:p.Asp124Gly
ENST00000680824.1:n.1587A>G
ENST00000681071.1:n.663A>G
ENST00000681166.1:n.1418A>G
ENST00000681341.1:n.1512A>G
ENST00000681640.1:n.465A>G
ENST00000681948.1:c.626A>G	ENSP00000505991.1:p.Asp209Gly
ENST00000358971.7:c.*169A>G	ENSP00000351857.3:n.*169A>G
ENST00000382103.6:c.371A>G	ENSP00000371535.2:p.Asp124Gly
ENST00000514585.5:c.*72A>G	ENSP00000421880.1:n.*72A>G
NM_016955.3:c.371A>G	NP_058651.3:p.Asp124Gly
XM_005248168.2:c.134A>G	XP_005248225.1:p.Asp45Gly
XM_006713965.2:c.191A>G	XP_006714028.1:p.Asp64Gly
XM_011513846.1:c.368A>G	XP_011512148.1:p.Asp123Gly
XM_011513847.1:c.338A>G	XP_011512149.1:p.Asp113Gly
XM_011513848.1:c.191A>G	XP_011512150.1:p.Asp64Gly
XM_011513846.2:c.368A>G	XP_011512148.1:p.Asp123Gly
XM_011513847.2:c.338A>G	XP_011512149.1:p.Asp113Gly
XM_017008277.1:c.626A>G	XP_016863766.1:p.Asp209Gly
XM_017008278.1:c.-53A>G	XP_016863767.1:n.-53A>G
NM_016955.4:c.371A>G MANE Select	NP_058651.3:p.Asp124Gly