Canonical Allele Identifier: CA438732335

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25144858-A-C
• MyVariant Identifiers: chr4:g.25146480A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144858A>C , CM000666.2:g.25144858A>C	GRCh38
NC_000004.11:g.25146480A>C , CM000666.1:g.25146480A>C	GRCh37
NC_000004.10:g.24755578A>C	NCBI36
NG_028222.1:g.20725T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.942T>G MANE Select	ENSP00000371535.2:p.Ala314=
ENST00000680581.1:c.942T>G	ENSP00000506483.1:p.Ala314=
ENST00000680824.1:n.2158T>G
ENST00000681071.1:n.1234T>G
ENST00000681341.1:n.2083T>G
ENST00000681948.1:c.1197T>G	ENSP00000505991.1:p.Ala399=
ENST00000358971.7:c.*740T>G	ENSP00000351857.3:n.*740T>G
ENST00000382103.6:c.942T>G	ENSP00000371535.2:p.Ala314=
ENST00000503150.1:c.224T>G
ENST00000505513.1:n.242T>G
ENST00000514585.5:c.*643T>G	ENSP00000421880.1:n.*643T>G
NM_016955.3:c.942T>G	NP_058651.3:p.Ala314=
XM_005248168.2:c.705T>G	XP_005248225.1:p.Ala235=
XM_006713965.2:c.762T>G	XP_006714028.1:p.Ala254=
XM_011513846.1:c.939T>G	XP_011512148.1:p.Ala313=
XM_011513847.1:c.909T>G	XP_011512149.1:p.Ala303=
XM_011513848.1:c.762T>G	XP_011512150.1:p.Ala254=
XM_011513846.2:c.939T>G	XP_011512148.1:p.Ala313=
XM_011513847.2:c.909T>G	XP_011512149.1:p.Ala303=
XM_017008277.1:c.1197T>G	XP_016863766.1:p.Ala399=
XM_017008278.1:c.519T>G	XP_016863767.1:p.Ala173=
NM_016955.4:c.942T>G MANE Select	NP_058651.3:p.Ala314=