Canonical Allele Identifier: CA1445223163
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144732T= , CM000666.2:g.25144732T= GRCh38
NC_000004.11:g.25146354T= , CM000666.1:g.25146354T= GRCh37
NC_000004.10:g.24755452T= NCBI36
NG_028222.1:g.20851A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382103.7:c.1026+42A= MANE Select ENSP00000371535.2:n.1026+42A=
ENST00000680581.1:c.1026+42A= ENSP00000506483.1:n.1026+42A=
ENST00000680824.1:n.2242+42A=
ENST00000681071.1:n.1318+42A=
ENST00000681341.1:n.2167+42A=
ENST00000681948.1:c.1281+42A= ENSP00000505991.1:n.1281+42A=
ENST00000358971.7:c.*824+42A= ENSP00000351857.3:n.*824+42A=
ENST00000382103.6:c.1026+42A= ENSP00000371535.2:n.1026+42A=
ENST00000503150.1:c.308+42A=
ENST00000505513.1:n.326+42A=
ENST00000514585.5:c.*727+42A= ENSP00000421880.1:n.*727+42A=
NM_016955.3:c.1026+42A= NP_058651.3:n.1026+42A=
XM_005248168.2:c.789+42A= XP_005248225.1:n.789+42A=
XM_006713965.2:c.846+42A= XP_006714028.1:n.846+42A=
XM_011513846.1:c.1023+42A= XP_011512148.1:n.1023+42A=
XM_011513847.1:c.993+42A= XP_011512149.1:n.993+42A=
XM_011513848.1:c.846+42A= XP_011512150.1:n.846+42A=
XM_011513846.2:c.1023+42A= XP_011512148.1:n.1023+42A=
XM_011513847.2:c.993+42A= XP_011512149.1:n.993+42A=
XM_017008277.1:c.1281+42A= XP_016863766.1:n.1281+42A=
XM_017008278.1:c.603+42A= XP_016863767.1:n.603+42A=
NM_016955.4:c.1026+42A= MANE Select NP_058651.3:n.1026+42A=