Canonical Allele Identifier: CA1675959361
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114815G= , CM000668.2:g.158114815G= GRCh38
NC_000006.11:g.158535847G= , CM000668.1:g.158535847G= GRCh37
NC_000006.10:g.158455835G= NCBI36
NG_032889.1:g.58466C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1378C= ENSP00000475855.1:n.*1378C=
ENST00000642244.1:c.1568C= ENSP00000493554.1:p.Ser523=
ENST00000642903.1:c.1658C= ENSP00000493559.1:p.Ser553=
ENST00000644972.1:c.1658C= ENSP00000496451.1:p.Ser553=
ENST00000645077.1:c.*1279C= ENSP00000496113.1:n.*1279C=
ENST00000645172.1:c.*1360C= ENSP00000495367.1:n.*1360C=
ENST00000646190.1:n.2989C=
ENST00000646208.1:c.1394C= ENSP00000493723.1:p.Ser465=
ENST00000646410.1:c.1529C= ENSP00000494205.1:p.Ser510=
ENST00000646562.1:c.*1492C= ENSP00000496087.1:n.*1492C=
ENST00000647468.2:c.1658C= MANE Select ENSP00000496731.1:p.Ser553=
ENST00000648111.1:c.*1346C= ENSP00000497275.1:n.*1346C=
ENST00000367101.5:c.*106C= ENSP00000356068.1:n.*106C=
ENST00000367104.7:c.1658C= ENSP00000356071.3:p.Ser553=
ENST00000435180.5:c.383C= ENSP00000391168.1:p.Ser128=
ENST00000606965.5:c.*219C= ENSP00000475808.1:n.*219C=
ENST00000607071.5:c.*1592C= ENSP00000475855.1:n.*1592C=
ENST00000607742.5:c.*2936C= ENSP00000475523.1:n.*2936C=
NM_032861.3:c.1658C= NP_116250.3:p.Ser553=
NR_073096.1:n.1591C=
XM_006715586.1:c.1448C= XP_006715649.1:p.Ser483=
XM_011536196.1:c.1637C= XP_011534498.1:p.Ser546=
XM_011536197.1:c.1544C= XP_011534499.1:p.Ser515=
XM_011536198.1:c.1448C= XP_011534500.1:p.Ser483=
XM_006715586.3:c.1448C= XP_006715649.1:p.Ser483=
XM_011536196.3:c.1637C= XP_011534498.1:p.Ser546=
XM_011536198.3:c.1448C= XP_011534500.1:p.Ser483=
XM_024446573.1:c.1658C= XP_024302341.1:p.Ser553=
XR_001743697.2:n.1689C=
XR_942606.2:n.1740C=
NM_032861.4:c.1658C= MANE Select NP_116250.3:p.Ser553=
NR_073096.2:n.1573C=