Canonical Allele Identifier: CA1675959577
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158115072T= , CM000668.2:g.158115072T= GRCh38
NC_000006.11:g.158536104T= , CM000668.1:g.158536104T= GRCh37
NC_000006.10:g.158456092T= NCBI36
NG_032889.1:g.58209A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.714-101A= ENSP00000391168.2:n.714-101A=
ENST00000607071.6:c.*1222-101A= ENSP00000475855.1:n.*1222-101A=
ENST00000642244.1:c.1412-101A= ENSP00000493554.1:n.1412-101A=
ENST00000642903.1:c.1502-101A= ENSP00000493559.1:n.1502-101A=
ENST00000644972.1:c.1502-101A= ENSP00000496451.1:n.1502-101A=
ENST00000645077.1:c.*1123-101A= ENSP00000496113.1:n.*1123-101A=
ENST00000645172.1:c.*1204-101A= ENSP00000495367.1:n.*1204-101A=
ENST00000646190.1:n.2833-101A=
ENST00000646208.1:c.1238-101A= ENSP00000493723.1:n.1238-101A=
ENST00000646410.1:c.1373-101A= ENSP00000494205.1:n.1373-101A=
ENST00000646562.1:c.*1336-101A= ENSP00000496087.1:n.*1336-101A=
ENST00000647468.2:c.1502-101A= MANE Select ENSP00000496731.1:n.1502-101A=
ENST00000648111.1:c.*1190-101A= ENSP00000497275.1:n.*1190-101A=
ENST00000367101.5:c.1546-101A= ENSP00000356068.1:n.1546-101A=
ENST00000367104.7:c.1502-101A= ENSP00000356071.3:n.1502-101A=
ENST00000435180.5:c.227-101A= ENSP00000391168.1:n.227-101A=
ENST00000606965.5:c.*63-101A= ENSP00000475808.1:n.*63-101A=
ENST00000607071.5:c.*1436-101A= ENSP00000475855.1:n.*1436-101A=
ENST00000607742.5:c.*2780-101A= ENSP00000475523.1:n.*2780-101A=
NM_032861.3:c.1502-101A= NP_116250.3:n.1502-101A=
NR_073096.1:n.1435-101A=
XM_006715586.1:c.1292-101A= XP_006715649.1:n.1292-101A=
XM_011536196.1:c.1481-101A= XP_011534498.1:n.1481-101A=
XM_011536197.1:c.1388-101A= XP_011534499.1:n.1388-101A=
XM_011536198.1:c.1292-101A= XP_011534500.1:n.1292-101A=
XM_006715586.3:c.1292-101A= XP_006715649.1:n.1292-101A=
XM_011536196.3:c.1481-101A= XP_011534498.1:n.1481-101A=
XM_011536198.3:c.1292-101A= XP_011534500.1:n.1292-101A=
XM_024446573.1:c.1502-101A= XP_024302341.1:n.1502-101A=
XR_001743697.2:n.1533-101A=
XR_942606.2:n.1584-101A=
NM_032861.4:c.1502-101A= MANE Select NP_116250.3:n.1502-101A=
NR_073096.2:n.1417-101A=