Canonical Allele Identifier: CA356536906

Gene: SEPSECS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.959T>C MANE Select	ENSP00000371535.2:p.Leu320Ser
ENST00000680581.1:c.959T>C	ENSP00000506483.1:p.Leu320Ser
ENST00000680824.1:n.2175T>C
ENST00000681071.1:n.1251T>C
ENST00000681341.1:n.2100T>C
ENST00000681948.1:c.1214T>C	ENSP00000505991.1:p.Leu405Ser
ENST00000358971.7:c.*757T>C	ENSP00000351857.3:n.*757T>C
ENST00000382103.6:c.959T>C	ENSP00000371535.2:p.Leu320Ser
ENST00000503150.1:c.241T>C
ENST00000505513.1:n.259T>C
ENST00000514585.5:c.*660T>C	ENSP00000421880.1:n.*660T>C
NM_016955.3:c.959T>C	NP_058651.3:p.Leu320Ser
XM_005248168.2:c.722T>C	XP_005248225.1:p.Leu241Ser
XM_006713965.2:c.779T>C	XP_006714028.1:p.Leu260Ser
XM_011513846.1:c.956T>C	XP_011512148.1:p.Leu319Ser
XM_011513847.1:c.926T>C	XP_011512149.1:p.Leu309Ser
XM_011513848.1:c.779T>C	XP_011512150.1:p.Leu260Ser
XM_011513846.2:c.956T>C	XP_011512148.1:p.Leu319Ser
XM_011513847.2:c.926T>C	XP_011512149.1:p.Leu309Ser
XM_017008277.1:c.1214T>C	XP_016863766.1:p.Leu405Ser
XM_017008278.1:c.536T>C	XP_016863767.1:p.Leu179Ser
NM_016955.4:c.959T>C MANE Select	NP_058651.3:p.Leu320Ser