Canonical Allele Identifier: CA438732712

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158506A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156884A>C , CM000666.2:g.25156884A>C	GRCh38
NC_000004.11:g.25158506A>C , CM000666.1:g.25158506A>C	GRCh37
NC_000004.10:g.24767604A>C	NCBI36
NG_028222.1:g.8699T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.360T>G MANE Select	ENSP00000371535.2:p.Ser120=
ENST00000680581.1:c.360T>G	ENSP00000506483.1:p.Ser120=
ENST00000680824.1:n.1576T>G
ENST00000681071.1:n.652T>G
ENST00000681166.1:n.1407T>G
ENST00000681341.1:n.1501T>G
ENST00000681640.1:n.454T>G
ENST00000681948.1:c.615T>G	ENSP00000505991.1:p.Ser205=
ENST00000358971.7:c.*158T>G	ENSP00000351857.3:n.*158T>G
ENST00000382103.6:c.360T>G	ENSP00000371535.2:p.Ser120=
ENST00000514585.5:c.*61T>G	ENSP00000421880.1:n.*61T>G
NM_016955.3:c.360T>G	NP_058651.3:p.Ser120=
XM_005248168.2:c.123T>G	XP_005248225.1:p.Ser41=
XM_006713965.2:c.180T>G	XP_006714028.1:p.Ser60=
XM_011513846.1:c.357T>G	XP_011512148.1:p.Ser119=
XM_011513847.1:c.327T>G	XP_011512149.1:p.Ser109=
XM_011513848.1:c.180T>G	XP_011512150.1:p.Ser60=
XM_011513846.2:c.357T>G	XP_011512148.1:p.Ser119=
XM_011513847.2:c.327T>G	XP_011512149.1:p.Ser109=
XM_017008277.1:c.615T>G	XP_016863766.1:p.Ser205=
XM_017008278.1:c.-64T>G	XP_016863767.1:n.-64T>G
NM_016955.4:c.360T>G MANE Select	NP_058651.3:p.Ser120=