Canonical Allele Identifier: CA645560967
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114939_158114940del , CM000668.2:g.158114939_158114940del GRCh38
NC_000006.11:g.158535971_158535972del , CM000668.1:g.158535971_158535972del GRCh37
NC_000006.10:g.158455959_158455960del NCBI36
NG_032889.1:g.58343_58344del

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.747_748del ENSP00000391168.2:n.747_748del
ENST00000607071.6:c.*1255_*1256del ENSP00000475855.1:n.*1255_*1256del
ENST00000642244.1:c.1445_1446del ENSP00000493554.1:p.Ser482TyrfsTer19
ENST00000642903.1:c.1535_1536del ENSP00000493559.1:p.Ser512TyrfsTer19
ENST00000644972.1:c.1535_1536del ENSP00000496451.1:p.Ser512TyrfsTer19
ENST00000645077.1:c.*1156_*1157del ENSP00000496113.1:n.*1156_*1157del
ENST00000645172.1:c.*1237_*1238del ENSP00000495367.1:n.*1237_*1238del
ENST00000646190.1:n.2866_2867del
ENST00000646208.1:c.1271_1272del ENSP00000493723.1:p.Ser424TyrfsTer19
ENST00000646410.1:c.1406_1407del ENSP00000494205.1:p.Ser469TyrfsTer19
ENST00000646562.1:c.*1369_*1370del ENSP00000496087.1:n.*1369_*1370del
ENST00000647468.2:c.1535_1536del MANE Select ENSP00000496731.1:p.Ser512TyrfsTer19
ENST00000648111.1:c.*1223_*1224del ENSP00000497275.1:n.*1223_*1224del
ENST00000367101.5:c.1579_1580del ENSP00000356068.1:p.Leu527ThrfsTer?
ENST00000367104.7:c.1535_1536del ENSP00000356071.3:p.Ser512TyrfsTer19
ENST00000435180.5:c.260_261del ENSP00000391168.1:p.Ser87TyrfsTer19
ENST00000606965.5:c.*96_*97del ENSP00000475808.1:n.*96_*97del
ENST00000607071.5:c.*1469_*1470del ENSP00000475855.1:n.*1469_*1470del
ENST00000607742.5:c.*2813_*2814del ENSP00000475523.1:n.*2813_*2814del
NM_032861.3:c.1535_1536del NP_116250.3:p.Ser512TyrfsTer19
NR_073096.1:n.1468_1469del
XM_006715586.1:c.1325_1326del XP_006715649.1:p.Ser442TyrfsTer19
XM_011536196.1:c.1514_1515del XP_011534498.1:p.Ser505TyrfsTer19
XM_011536197.1:c.1421_1422del XP_011534499.1:p.Ser474TyrfsTer19
XM_011536198.1:c.1325_1326del XP_011534500.1:p.Ser442TyrfsTer19
XM_006715586.3:c.1325_1326del XP_006715649.1:p.Ser442TyrfsTer19
XM_011536196.3:c.1514_1515del XP_011534498.1:p.Ser505TyrfsTer19
XM_011536198.3:c.1325_1326del XP_011534500.1:p.Ser442TyrfsTer19
XM_024446573.1:c.1535_1536del XP_024302341.1:p.Ser512TyrfsTer19
XR_001743697.2:n.1566_1567del
XR_942606.2:n.1617_1618del
NM_032861.4:c.1535_1536del MANE Select NP_116250.3:p.Ser512TyrfsTer19
NR_073096.2:n.1450_1451del