Canonical Allele Identifier: CA2680956501
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114688_158114689insGAGATAATGCATTCAAGGAA , CM000668.2:g.158114688_158114689insGAGATAATGCATTCAAGGAA GRCh38
NC_000006.11:g.158535720_158535721insGAGATAATGCATTCAAGGAA , CM000668.1:g.158535720_158535721insGAGATAATGCATTCAAGGAA GRCh37
NC_000006.10:g.158455708_158455709insGAGATAATGCATTCAAGGAA NCBI36
NG_032889.1:g.58592_58593insTTCCTTGAATGCATTATCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1404+100_*1404+101insTTCCTTGAATGCATTATCTC ENSP00000475855.1:n.*1404+100_*1404+101insTTCCTTGAATGCATTATCT...
ENST00000642244.1:c.1594+100_1594+101insTTCCTTGAATGCATTATCTC ENSP00000493554.1:n.1594+100_1594+101insTTCCTTGAATGCATTATCTC
ENST00000642903.1:c.*20_*21insTTCCTTGAATGCATTATCTC ENSP00000493559.1:n.*20_*21insTTCCTTGAATGCATTATCTC
ENST00000644972.1:c.1684+100_1684+101insTTCCTTGAATGCATTATCTC ENSP00000496451.1:n.1684+100_1684+101insTTCCTTGAATGCATTATCTC
ENST00000645077.1:c.*1305+100_*1305+101insTTCCTTGAATGCATTATCTC ENSP00000496113.1:n.*1305+100_*1305+101insTTCCTTGAATGCATTATCT...
ENST00000645172.1:c.*1386+100_*1386+101insTTCCTTGAATGCATTATCTC ENSP00000495367.1:n.*1386+100_*1386+101insTTCCTTGAATGCATTATCT...
ENST00000646190.1:n.3015+100_3015+101insTTCCTTGAATGCATTATCTC
ENST00000646208.1:c.1420+100_1420+101insTTCCTTGAATGCATTATCTC ENSP00000493723.1:n.1420+100_1420+101insTTCCTTGAATGCATTATCTC
ENST00000646410.1:c.1555+100_1555+101insTTCCTTGAATGCATTATCTC ENSP00000494205.1:n.1555+100_1555+101insTTCCTTGAATGCATTATCTC
ENST00000646562.1:c.*1618_*1619insTTCCTTGAATGCATTATCTC ENSP00000496087.1:n.*1618_*1619insTTCCTTGAATGCATTATCTC
ENST00000647468.2:c.1684+100_1684+101insTTCCTTGAATGCATTATCTC MANE Select ENSP00000496731.1:n.1684+100_1684+101insTTCCTTGAATGCATTATCTC
ENST00000648111.1:c.*1372+100_*1372+101insTTCCTTGAATGCATTATCTC ENSP00000497275.1:n.*1372+100_*1372+101insTTCCTTGAATGCATTATCT...
ENST00000367104.7:c.1684+100_1684+101insTTCCTTGAATGCATTATCTC ENSP00000356071.3:n.1684+100_1684+101insTTCCTTGAATGCATTATCTC
ENST00000606965.5:c.*345_*346insTTCCTTGAATGCATTATCTC ENSP00000475808.1:n.*345_*346insTTCCTTGAATGCATTATCTC
ENST00000607071.5:c.*1618+100_*1618+101insTTCCTTGAATGCATTATCTC ENSP00000475855.1:n.*1618+100_*1618+101insTTCCTTGAATGCATTATCT...
ENST00000607742.5:c.*2962+100_*2962+101insTTCCTTGAATGCATTATCTC ENSP00000475523.1:n.*2962+100_*2962+101insTTCCTTGAATGCATTATCT...
NM_032861.3:c.1684+100_1684+101insTTCCTTGAATGCATTATCTC NP_116250.3:n.1684+100_1684+101insTTCCTTGAATGCATTATCTC
NR_073096.1:n.1717_1718insTTCCTTGAATGCATTATCTC
XM_006715586.1:c.1474+100_1474+101insTTCCTTGAATGCATTATCTC XP_006715649.1:n.1474+100_1474+101insTTCCTTGAATGCATTATCTC
XM_011536196.1:c.1663+100_1663+101insTTCCTTGAATGCATTATCTC XP_011534498.1:n.1663+100_1663+101insTTCCTTGAATGCATTATCTC
XM_011536197.1:c.1570+100_1570+101insTTCCTTGAATGCATTATCTC XP_011534499.1:n.1570+100_1570+101insTTCCTTGAATGCATTATCTC
XM_011536198.1:c.1474+100_1474+101insTTCCTTGAATGCATTATCTC XP_011534500.1:n.1474+100_1474+101insTTCCTTGAATGCATTATCTC
XM_006715586.3:c.1474+100_1474+101insTTCCTTGAATGCATTATCTC XP_006715649.1:n.1474+100_1474+101insTTCCTTGAATGCATTATCTC
XM_011536196.3:c.1663+100_1663+101insTTCCTTGAATGCATTATCTC XP_011534498.1:n.1663+100_1663+101insTTCCTTGAATGCATTATCTC
XM_011536198.3:c.1474+100_1474+101insTTCCTTGAATGCATTATCTC XP_011534500.1:n.1474+100_1474+101insTTCCTTGAATGCATTATCTC
XM_024446573.1:c.1684+100_1684+101insTTCCTTGAATGCATTATCTC XP_024302341.1:n.1684+100_1684+101insTTCCTTGAATGCATTATCTC
XR_001743697.2:n.1715+100_1715+101insTTCCTTGAATGCATTATCTC
XR_942606.2:n.1766+100_1766+101insTTCCTTGAATGCATTATCTC
NM_032861.4:c.1684+100_1684+101insTTCCTTGAATGCATTATCTC MANE Select NP_116250.3:n.1684+100_1684+101insTTCCTTGAATGCATTATCTC
NR_073096.2:n.1699_1700insTTCCTTGAATGCATTATCTC