Canonical Allele Identifier: CA1445223152
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144716T= , CM000666.2:g.25144716T= GRCh38
NC_000004.11:g.25146338T= , CM000666.1:g.25146338T= GRCh37
NC_000004.10:g.24755436T= NCBI36
NG_028222.1:g.20867A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382103.7:c.1026+58A= MANE Select ENSP00000371535.2:n.1026+58A=
ENST00000680581.1:c.1026+58A= ENSP00000506483.1:n.1026+58A=
ENST00000680824.1:n.2242+58A=
ENST00000681071.1:n.1318+58A=
ENST00000681341.1:n.2167+58A=
ENST00000681948.1:c.1281+58A= ENSP00000505991.1:n.1281+58A=
ENST00000358971.7:c.*824+58A= ENSP00000351857.3:n.*824+58A=
ENST00000382103.6:c.1026+58A= ENSP00000371535.2:n.1026+58A=
ENST00000503150.1:c.308+58A=
ENST00000505513.1:n.326+58A=
ENST00000514585.5:c.*727+58A= ENSP00000421880.1:n.*727+58A=
NM_016955.3:c.1026+58A= NP_058651.3:n.1026+58A=
XM_005248168.2:c.789+58A= XP_005248225.1:n.789+58A=
XM_006713965.2:c.846+58A= XP_006714028.1:n.846+58A=
XM_011513846.1:c.1023+58A= XP_011512148.1:n.1023+58A=
XM_011513847.1:c.993+58A= XP_011512149.1:n.993+58A=
XM_011513848.1:c.846+58A= XP_011512150.1:n.846+58A=
XM_011513846.2:c.1023+58A= XP_011512148.1:n.1023+58A=
XM_011513847.2:c.993+58A= XP_011512149.1:n.993+58A=
XM_017008277.1:c.1281+58A= XP_016863766.1:n.1281+58A=
XM_017008278.1:c.603+58A= XP_016863767.1:n.603+58A=
NM_016955.4:c.1026+58A= MANE Select NP_058651.3:n.1026+58A=