Canonical Allele Identifier: CA1675955811
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158146878A= , CM000668.2:g.158146878A= GRCh38
NC_000006.11:g.158567910A= , CM000668.1:g.158567910A= GRCh37
NC_000006.10:g.158487898A= NCBI36
NG_032889.1:g.26403T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*225T= ENSP00000475855.1:n.*225T=
ENST00000642244.1:c.301T= ENSP00000493554.1:p.Cys101=
ENST00000642903.1:c.391T= ENSP00000493559.1:p.Cys131=
ENST00000643093.1:n.441T=
ENST00000644972.1:c.391T= ENSP00000496451.1:p.Cys131=
ENST00000645077.1:c.*225T= ENSP00000496113.1:n.*225T=
ENST00000645172.1:c.*189+1987T= ENSP00000495367.1:n.*189+1987T=
ENST00000646190.1:n.1622T=
ENST00000646208.1:c.127T= ENSP00000493723.1:p.Cys43=
ENST00000646410.1:c.262T= ENSP00000494205.1:p.Cys88=
ENST00000646562.1:c.*225T= ENSP00000496087.1:n.*225T=
ENST00000647468.2:c.391T= MANE Select ENSP00000496731.1:p.Cys131=
ENST00000648111.1:c.*35T= ENSP00000497275.1:n.*35T=
ENST00000367101.5:c.391T= ENSP00000356068.1:p.Cys131=
ENST00000367104.7:c.391T= ENSP00000356071.3:p.Cys131=
ENST00000606965.5:c.391T= ENSP00000475808.1:p.Cys131=
ENST00000607000.1:c.391T= ENSP00000475788.1:p.Cys131=
ENST00000607071.5:c.*225T= ENSP00000475855.1:n.*225T=
ENST00000607742.5:c.*225T= ENSP00000475523.1:n.*225T=
NM_032861.3:c.391T= NP_116250.3:p.Cys131=
NR_073096.1:n.533T=
XM_006715586.1:c.181T= XP_006715649.1:p.Cys61=
XM_011536196.1:c.370T= XP_011534498.1:p.Cys124=
XM_011536197.1:c.391T= XP_011534499.1:p.Cys131=
XM_011536198.1:c.181T= XP_011534500.1:p.Cys61=
XR_942606.1:n.392T=
XM_006715586.3:c.181T= XP_006715649.1:p.Cys61=
XM_011536196.3:c.370T= XP_011534498.1:p.Cys124=
XM_011536198.3:c.181T= XP_011534500.1:p.Cys61=
XM_024446573.1:c.391T= XP_024302341.1:p.Cys131=
XR_001743697.2:n.472T=
XR_942606.2:n.523T=
NM_032861.4:c.391T= MANE Select NP_116250.3:p.Cys131=
NR_073096.2:n.515T=