Canonical Allele Identifier: CA356536904

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146463A>C (hg19) ; chr4:g.25144841A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144841A>C , CM000666.2:g.25144841A>C	GRCh38
NC_000004.11:g.25146463A>C , CM000666.1:g.25146463A>C	GRCh37
NC_000004.10:g.24755561A>C	NCBI36
NG_028222.1:g.20742T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.959T>G MANE Select	ENSP00000371535.2:p.Leu320Ter
ENST00000680581.1:c.959T>G	ENSP00000506483.1:p.Leu320Ter
ENST00000680824.1:n.2175T>G
ENST00000681071.1:n.1251T>G
ENST00000681341.1:n.2100T>G
ENST00000681948.1:c.1214T>G	ENSP00000505991.1:p.Leu405Ter
ENST00000358971.7:c.*757T>G	ENSP00000351857.3:n.*757T>G
ENST00000382103.6:c.959T>G	ENSP00000371535.2:p.Leu320Ter
ENST00000503150.1:c.241T>G
ENST00000505513.1:n.259T>G
ENST00000514585.5:c.*660T>G	ENSP00000421880.1:n.*660T>G
NM_016955.3:c.959T>G	NP_058651.3:p.Leu320Ter
XM_005248168.2:c.722T>G	XP_005248225.1:p.Leu241Ter
XM_006713965.2:c.779T>G	XP_006714028.1:p.Leu260Ter
XM_011513846.1:c.956T>G	XP_011512148.1:p.Leu319Ter
XM_011513847.1:c.926T>G	XP_011512149.1:p.Leu309Ter
XM_011513848.1:c.779T>G	XP_011512150.1:p.Leu260Ter
XM_011513846.2:c.956T>G	XP_011512148.1:p.Leu319Ter
XM_011513847.2:c.926T>G	XP_011512149.1:p.Leu309Ter
XM_017008277.1:c.1214T>G	XP_016863766.1:p.Leu405Ter
XM_017008278.1:c.536T>G	XP_016863767.1:p.Leu179Ter
NM_016955.4:c.959T>G MANE Select	NP_058651.3:p.Leu320Ter