Canonical Allele Identifier: CA1675959477
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114934C= , CM000668.2:g.158114934C= GRCh38
NC_000006.11:g.158535966C= , CM000668.1:g.158535966C= GRCh37
NC_000006.10:g.158455954C= NCBI36
NG_032889.1:g.58347G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.751G= ENSP00000391168.2:n.751G=
ENST00000607071.6:c.*1259G= ENSP00000475855.1:n.*1259G=
ENST00000642244.1:c.1449G= ENSP00000493554.1:p.Thr483=
ENST00000642903.1:c.1539G= ENSP00000493559.1:p.Thr513=
ENST00000644972.1:c.1539G= ENSP00000496451.1:p.Thr513=
ENST00000645077.1:c.*1160G= ENSP00000496113.1:n.*1160G=
ENST00000645172.1:c.*1241G= ENSP00000495367.1:n.*1241G=
ENST00000646190.1:n.2870G=
ENST00000646208.1:c.1275G= ENSP00000493723.1:p.Thr425=
ENST00000646410.1:c.1410G= ENSP00000494205.1:p.Thr470=
ENST00000646562.1:c.*1373G= ENSP00000496087.1:n.*1373G=
ENST00000647468.2:c.1539G= MANE Select ENSP00000496731.1:p.Thr513=
ENST00000648111.1:c.*1227G= ENSP00000497275.1:n.*1227G=
ENST00000367101.5:c.1583G= ENSP00000356068.1:p.Arg528=
ENST00000367104.7:c.1539G= ENSP00000356071.3:p.Thr513=
ENST00000435180.5:c.264G= ENSP00000391168.1:p.Thr88=
ENST00000606965.5:c.*100G= ENSP00000475808.1:n.*100G=
ENST00000607071.5:c.*1473G= ENSP00000475855.1:n.*1473G=
ENST00000607742.5:c.*2817G= ENSP00000475523.1:n.*2817G=
NM_032861.3:c.1539G= NP_116250.3:p.Thr513=
NR_073096.1:n.1472G=
XM_006715586.1:c.1329G= XP_006715649.1:p.Thr443=
XM_011536196.1:c.1518G= XP_011534498.1:p.Thr506=
XM_011536197.1:c.1425G= XP_011534499.1:p.Thr475=
XM_011536198.1:c.1329G= XP_011534500.1:p.Thr443=
XM_006715586.3:c.1329G= XP_006715649.1:p.Thr443=
XM_011536196.3:c.1518G= XP_011534498.1:p.Thr506=
XM_011536198.3:c.1329G= XP_011534500.1:p.Thr443=
XM_024446573.1:c.1539G= XP_024302341.1:p.Thr513=
XR_001743697.2:n.1570G=
XR_942606.2:n.1621G=
NM_032861.4:c.1539G= MANE Select NP_116250.3:p.Thr513=
NR_073096.2:n.1454G=