Canonical Allele Identifier: CA1096370347
Gene: SERAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1784237912

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114752del , CM000668.2:g.158114752del GRCh38
NC_000006.11:g.158535784del , CM000668.1:g.158535784del GRCh37
NC_000006.10:g.158455772del NCBI36
NG_032889.1:g.58530del

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1404+38del ENSP00000475855.1:n.*1404+38del
ENST00000642244.1:c.1594+38del ENSP00000493554.1:n.1594+38del
ENST00000642903.1:c.1722del ENSP00000493559.1:p.Asn575ThrfsTer?
ENST00000644972.1:c.1684+38del ENSP00000496451.1:n.1684+38del
ENST00000645077.1:c.*1305+38del ENSP00000496113.1:n.*1305+38del
ENST00000645172.1:c.*1386+38del ENSP00000495367.1:n.*1386+38del
ENST00000646190.1:n.3015+38del
ENST00000646208.1:c.1420+38del ENSP00000493723.1:n.1420+38del
ENST00000646410.1:c.1555+38del ENSP00000494205.1:n.1555+38del
ENST00000646562.1:c.*1556del ENSP00000496087.1:n.*1556del
ENST00000647468.2:c.1684+38del MANE Select ENSP00000496731.1:n.1684+38del
ENST00000648111.1:c.*1372+38del ENSP00000497275.1:n.*1372+38del
ENST00000367101.5:c.*170del ENSP00000356068.1:n.*170del
ENST00000367104.7:c.1684+38del ENSP00000356071.3:n.1684+38del
ENST00000435180.5:c.447del ENSP00000391168.1:p.Asn150ThrfsTer?
ENST00000606965.5:c.*283del ENSP00000475808.1:n.*283del
ENST00000607071.5:c.*1618+38del ENSP00000475855.1:n.*1618+38del
ENST00000607742.5:c.*2962+38del ENSP00000475523.1:n.*2962+38del
NM_032861.3:c.1684+38del NP_116250.3:n.1684+38del
NR_073096.1:n.1655del
XM_006715586.1:c.1474+38del XP_006715649.1:n.1474+38del
XM_011536196.1:c.1663+38del XP_011534498.1:n.1663+38del
XM_011536197.1:c.1570+38del XP_011534499.1:n.1570+38del
XM_011536198.1:c.1474+38del XP_011534500.1:n.1474+38del
XM_006715586.3:c.1474+38del XP_006715649.1:n.1474+38del
XM_011536196.3:c.1663+38del XP_011534498.1:n.1663+38del
XM_011536198.3:c.1474+38del XP_011534500.1:n.1474+38del
XM_024446573.1:c.1684+38del XP_024302341.1:n.1684+38del
XR_001743697.2:n.1715+38del
XR_942606.2:n.1766+38del
NM_032861.4:c.1684+38del MANE Select NP_116250.3:n.1684+38del
NR_073096.2:n.1637del