Canonical Allele Identifier: CA1675959414
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114846A= , CM000668.2:g.158114846A= GRCh38
NC_000006.11:g.158535878A= , CM000668.1:g.158535878A= GRCh37
NC_000006.10:g.158455866A= NCBI36
NG_032889.1:g.58435T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.839T= ENSP00000391168.2:n.839T=
ENST00000607071.6:c.*1347T= ENSP00000475855.1:n.*1347T=
ENST00000642244.1:c.1537T= ENSP00000493554.1:p.Ser513=
ENST00000642903.1:c.1627T= ENSP00000493559.1:p.Ser543=
ENST00000644972.1:c.1627T= ENSP00000496451.1:p.Ser543=
ENST00000645077.1:c.*1248T= ENSP00000496113.1:n.*1248T=
ENST00000645172.1:c.*1329T= ENSP00000495367.1:n.*1329T=
ENST00000646190.1:n.2958T=
ENST00000646208.1:c.1363T= ENSP00000493723.1:p.Ser455=
ENST00000646410.1:c.1498T= ENSP00000494205.1:p.Ser500=
ENST00000646562.1:c.*1461T= ENSP00000496087.1:n.*1461T=
ENST00000647468.2:c.1627T= MANE Select ENSP00000496731.1:p.Ser543=
ENST00000648111.1:c.*1315T= ENSP00000497275.1:n.*1315T=
ENST00000367101.5:c.*75T= ENSP00000356068.1:n.*75T=
ENST00000367104.7:c.1627T= ENSP00000356071.3:p.Ser543=
ENST00000435180.5:c.352T= ENSP00000391168.1:p.Ser118=
ENST00000606965.5:c.*188T= ENSP00000475808.1:n.*188T=
ENST00000607071.5:c.*1561T= ENSP00000475855.1:n.*1561T=
ENST00000607742.5:c.*2905T= ENSP00000475523.1:n.*2905T=
NM_032861.3:c.1627T= NP_116250.3:p.Ser543=
NR_073096.1:n.1560T=
XM_006715586.1:c.1417T= XP_006715649.1:p.Ser473=
XM_011536196.1:c.1606T= XP_011534498.1:p.Ser536=
XM_011536197.1:c.1513T= XP_011534499.1:p.Ser505=
XM_011536198.1:c.1417T= XP_011534500.1:p.Ser473=
XM_006715586.3:c.1417T= XP_006715649.1:p.Ser473=
XM_011536196.3:c.1606T= XP_011534498.1:p.Ser536=
XM_011536198.3:c.1417T= XP_011534500.1:p.Ser473=
XM_024446573.1:c.1627T= XP_024302341.1:p.Ser543=
XR_001743697.2:n.1658T=
XR_942606.2:n.1709T=
NM_032861.4:c.1627T= MANE Select NP_116250.3:p.Ser543=
NR_073096.2:n.1542T=