Canonical Allele Identifier: CA1445223154
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144721T= , CM000666.2:g.25144721T= GRCh38
NC_000004.11:g.25146343T= , CM000666.1:g.25146343T= GRCh37
NC_000004.10:g.24755441T= NCBI36
NG_028222.1:g.20862A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382103.7:c.1026+53A= MANE Select ENSP00000371535.2:n.1026+53A=
ENST00000680581.1:c.1026+53A= ENSP00000506483.1:n.1026+53A=
ENST00000680824.1:n.2242+53A=
ENST00000681071.1:n.1318+53A=
ENST00000681341.1:n.2167+53A=
ENST00000681948.1:c.1281+53A= ENSP00000505991.1:n.1281+53A=
ENST00000358971.7:c.*824+53A= ENSP00000351857.3:n.*824+53A=
ENST00000382103.6:c.1026+53A= ENSP00000371535.2:n.1026+53A=
ENST00000503150.1:c.308+53A=
ENST00000505513.1:n.326+53A=
ENST00000514585.5:c.*727+53A= ENSP00000421880.1:n.*727+53A=
NM_016955.3:c.1026+53A= NP_058651.3:n.1026+53A=
XM_005248168.2:c.789+53A= XP_005248225.1:n.789+53A=
XM_006713965.2:c.846+53A= XP_006714028.1:n.846+53A=
XM_011513846.1:c.1023+53A= XP_011512148.1:n.1023+53A=
XM_011513847.1:c.993+53A= XP_011512149.1:n.993+53A=
XM_011513848.1:c.846+53A= XP_011512150.1:n.846+53A=
XM_011513846.2:c.1023+53A= XP_011512148.1:n.1023+53A=
XM_011513847.2:c.993+53A= XP_011512149.1:n.993+53A=
XM_017008277.1:c.1281+53A= XP_016863766.1:n.1281+53A=
XM_017008278.1:c.603+53A= XP_016863767.1:n.603+53A=
NM_016955.4:c.1026+53A= MANE Select NP_058651.3:n.1026+53A=