Canonical Allele Identifier: CA1675959331
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114795T= , CM000668.2:g.158114795T= GRCh38
NC_000006.11:g.158535827T= , CM000668.1:g.158535827T= GRCh37
NC_000006.10:g.158455815T= NCBI36
NG_032889.1:g.58486A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1398A= ENSP00000475855.1:n.*1398A=
ENST00000642244.1:c.1588A= ENSP00000493554.1:p.Ser530=
ENST00000642903.1:c.1678A= ENSP00000493559.1:p.Ser560=
ENST00000644972.1:c.1678A= ENSP00000496451.1:p.Ser560=
ENST00000645077.1:c.*1299A= ENSP00000496113.1:n.*1299A=
ENST00000645172.1:c.*1380A= ENSP00000495367.1:n.*1380A=
ENST00000646190.1:n.3009A=
ENST00000646208.1:c.1414A= ENSP00000493723.1:p.Ser472=
ENST00000646410.1:c.1549A= ENSP00000494205.1:p.Ser517=
ENST00000646562.1:c.*1512A= ENSP00000496087.1:n.*1512A=
ENST00000647468.2:c.1678A= MANE Select ENSP00000496731.1:p.Ser560=
ENST00000648111.1:c.*1366A= ENSP00000497275.1:n.*1366A=
ENST00000367101.5:c.*126A= ENSP00000356068.1:n.*126A=
ENST00000367104.7:c.1678A= ENSP00000356071.3:p.Ser560=
ENST00000435180.5:c.403A= ENSP00000391168.1:p.Ser135=
ENST00000606965.5:c.*239A= ENSP00000475808.1:n.*239A=
ENST00000607071.5:c.*1612A= ENSP00000475855.1:n.*1612A=
ENST00000607742.5:c.*2956A= ENSP00000475523.1:n.*2956A=
NM_032861.3:c.1678A= NP_116250.3:p.Ser560=
NR_073096.1:n.1611A=
XM_006715586.1:c.1468A= XP_006715649.1:p.Ser490=
XM_011536196.1:c.1657A= XP_011534498.1:p.Ser553=
XM_011536197.1:c.1564A= XP_011534499.1:p.Ser522=
XM_011536198.1:c.1468A= XP_011534500.1:p.Ser490=
XM_006715586.3:c.1468A= XP_006715649.1:p.Ser490=
XM_011536196.3:c.1657A= XP_011534498.1:p.Ser553=
XM_011536198.3:c.1468A= XP_011534500.1:p.Ser490=
XM_024446573.1:c.1678A= XP_024302341.1:p.Ser560=
XR_001743697.2:n.1709A=
XR_942606.2:n.1760A=
NM_032861.4:c.1678A= MANE Select NP_116250.3:p.Ser560=
NR_073096.2:n.1593A=