Canonical Allele Identifier: CA1675959392
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114834G= , CM000668.2:g.158114834G= GRCh38
NC_000006.11:g.158535866G= , CM000668.1:g.158535866G= GRCh37
NC_000006.10:g.158455854G= NCBI36
NG_032889.1:g.58447C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.851C= ENSP00000391168.2:n.851C=
ENST00000607071.6:c.*1359C= ENSP00000475855.1:n.*1359C=
ENST00000642244.1:c.1549C= ENSP00000493554.1:p.Arg517=
ENST00000642903.1:c.1639C= ENSP00000493559.1:p.Arg547=
ENST00000644972.1:c.1639C= ENSP00000496451.1:p.Arg547=
ENST00000645077.1:c.*1260C= ENSP00000496113.1:n.*1260C=
ENST00000645172.1:c.*1341C= ENSP00000495367.1:n.*1341C=
ENST00000646190.1:n.2970C=
ENST00000646208.1:c.1375C= ENSP00000493723.1:p.Arg459=
ENST00000646410.1:c.1510C= ENSP00000494205.1:p.Arg504=
ENST00000646562.1:c.*1473C= ENSP00000496087.1:n.*1473C=
ENST00000647468.2:c.1639C= MANE Select ENSP00000496731.1:p.Arg547=
ENST00000648111.1:c.*1327C= ENSP00000497275.1:n.*1327C=
ENST00000367101.5:c.*87C= ENSP00000356068.1:n.*87C=
ENST00000367104.7:c.1639C= ENSP00000356071.3:p.Arg547=
ENST00000435180.5:c.364C= ENSP00000391168.1:p.Arg122=
ENST00000606965.5:c.*200C= ENSP00000475808.1:n.*200C=
ENST00000607071.5:c.*1573C= ENSP00000475855.1:n.*1573C=
ENST00000607742.5:c.*2917C= ENSP00000475523.1:n.*2917C=
NM_032861.3:c.1639C= NP_116250.3:p.Arg547=
NR_073096.1:n.1572C=
XM_006715586.1:c.1429C= XP_006715649.1:p.Arg477=
XM_011536196.1:c.1618C= XP_011534498.1:p.Arg540=
XM_011536197.1:c.1525C= XP_011534499.1:p.Arg509=
XM_011536198.1:c.1429C= XP_011534500.1:p.Arg477=
XM_006715586.3:c.1429C= XP_006715649.1:p.Arg477=
XM_011536196.3:c.1618C= XP_011534498.1:p.Arg540=
XM_011536198.3:c.1429C= XP_011534500.1:p.Arg477=
XM_024446573.1:c.1639C= XP_024302341.1:p.Arg547=
XR_001743697.2:n.1670C=
XR_942606.2:n.1721C=
NM_032861.4:c.1639C= MANE Select NP_116250.3:p.Arg547=
NR_073096.2:n.1554C=