Canonical Allele Identifier: CA356536744

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146422A>C (hg19) ; chr4:g.25144800A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144800A>C , CM000666.2:g.25144800A>C	GRCh38
NC_000004.11:g.25146422A>C , CM000666.1:g.25146422A>C	GRCh37
NC_000004.10:g.24755520A>C	NCBI36
NG_028222.1:g.20783T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.1000T>G MANE Select	ENSP00000371535.2:p.Tyr334Asp
ENST00000680581.1:c.1000T>G	ENSP00000506483.1:p.Tyr334Asp
ENST00000680824.1:n.2216T>G
ENST00000681071.1:n.1292T>G
ENST00000681341.1:n.2141T>G
ENST00000681948.1:c.1255T>G	ENSP00000505991.1:p.Tyr419Asp
ENST00000358971.7:c.*798T>G	ENSP00000351857.3:n.*798T>G
ENST00000382103.6:c.1000T>G	ENSP00000371535.2:p.Tyr334Asp
ENST00000503150.1:c.282T>G
ENST00000505513.1:n.300T>G
ENST00000514585.5:c.*701T>G	ENSP00000421880.1:n.*701T>G
NM_016955.3:c.1000T>G	NP_058651.3:p.Tyr334Asp
XM_005248168.2:c.763T>G	XP_005248225.1:p.Tyr255Asp
XM_006713965.2:c.820T>G	XP_006714028.1:p.Tyr274Asp
XM_011513846.1:c.997T>G	XP_011512148.1:p.Tyr333Asp
XM_011513847.1:c.967T>G	XP_011512149.1:p.Tyr323Asp
XM_011513848.1:c.820T>G	XP_011512150.1:p.Tyr274Asp
XM_011513846.2:c.997T>G	XP_011512148.1:p.Tyr333Asp
XM_011513847.2:c.967T>G	XP_011512149.1:p.Tyr323Asp
XM_017008277.1:c.1255T>G	XP_016863766.1:p.Tyr419Asp
XM_017008278.1:c.577T>G	XP_016863767.1:p.Tyr193Asp
NM_016955.4:c.1000T>G MANE Select	NP_058651.3:p.Tyr334Asp