Canonical Allele Identifier: CA2680956644
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114718_158114719insGATAATACATTCAAGGAAG , CM000668.2:g.158114718_158114719insGATAATACATTCAAGGAAG GRCh38
NC_000006.11:g.158535750_158535751insGATAATACATTCAAGGAAG , CM000668.1:g.158535750_158535751insGATAATACATTCAAGGAAG GRCh37
NC_000006.10:g.158455738_158455739insGATAATACATTCAAGGAAG NCBI36
NG_032889.1:g.58562_58563insCTTCCTTGAATGTATTATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1404+70_*1404+71insCTTCCTTGAATGTATTATC ENSP00000475855.1:n.*1404+70_*1404+71insCTTCCTTGAATGTATTATC
ENST00000642244.1:c.1594+70_1594+71insCTTCCTTGAATGTATTATC ENSP00000493554.1:n.1594+70_1594+71insCTTCCTTGAATGTATTATC
ENST00000642903.1:c.1754_1755insCTTCCTTGAATGTATTATC ENSP00000493559.1:p.Leu586PhefsTer20
ENST00000644972.1:c.1684+70_1684+71insCTTCCTTGAATGTATTATC ENSP00000496451.1:n.1684+70_1684+71insCTTCCTTGAATGTATTATC
ENST00000645077.1:c.*1305+70_*1305+71insCTTCCTTGAATGTATTATC ENSP00000496113.1:n.*1305+70_*1305+71insCTTCCTTGAATGTATTATC
ENST00000645172.1:c.*1386+70_*1386+71insCTTCCTTGAATGTATTATC ENSP00000495367.1:n.*1386+70_*1386+71insCTTCCTTGAATGTATTATC
ENST00000646190.1:n.3015+70_3015+71insCTTCCTTGAATGTATTATC
ENST00000646208.1:c.1420+70_1420+71insCTTCCTTGAATGTATTATC ENSP00000493723.1:n.1420+70_1420+71insCTTCCTTGAATGTATTATC
ENST00000646410.1:c.1555+70_1555+71insCTTCCTTGAATGTATTATC ENSP00000494205.1:n.1555+70_1555+71insCTTCCTTGAATGTATTATC
ENST00000646562.1:c.*1588_*1589insCTTCCTTGAATGTATTATC ENSP00000496087.1:n.*1588_*1589insCTTCCTTGAATGTATTATC
ENST00000647468.2:c.1684+70_1684+71insCTTCCTTGAATGTATTATC MANE Select ENSP00000496731.1:n.1684+70_1684+71insCTTCCTTGAATGTATTATC
ENST00000648111.1:c.*1372+70_*1372+71insCTTCCTTGAATGTATTATC ENSP00000497275.1:n.*1372+70_*1372+71insCTTCCTTGAATGTATTATC
ENST00000367104.7:c.1684+70_1684+71insCTTCCTTGAATGTATTATC ENSP00000356071.3:n.1684+70_1684+71insCTTCCTTGAATGTATTATC
ENST00000435180.5:c.479_480insCTTCCTTGAATGTATTATC ENSP00000391168.1:p.Leu161PhefsTer?
ENST00000606965.5:c.*315_*316insCTTCCTTGAATGTATTATC ENSP00000475808.1:n.*315_*316insCTTCCTTGAATGTATTATC
ENST00000607071.5:c.*1618+70_*1618+71insCTTCCTTGAATGTATTATC ENSP00000475855.1:n.*1618+70_*1618+71insCTTCCTTGAATGTATTATC
ENST00000607742.5:c.*2962+70_*2962+71insCTTCCTTGAATGTATTATC ENSP00000475523.1:n.*2962+70_*2962+71insCTTCCTTGAATGTATTATC
NM_032861.3:c.1684+70_1684+71insCTTCCTTGAATGTATTATC NP_116250.3:n.1684+70_1684+71insCTTCCTTGAATGTATTATC
NR_073096.1:n.1687_1688insCTTCCTTGAATGTATTATC
XM_006715586.1:c.1474+70_1474+71insCTTCCTTGAATGTATTATC XP_006715649.1:n.1474+70_1474+71insCTTCCTTGAATGTATTATC
XM_011536196.1:c.1663+70_1663+71insCTTCCTTGAATGTATTATC XP_011534498.1:n.1663+70_1663+71insCTTCCTTGAATGTATTATC
XM_011536197.1:c.1570+70_1570+71insCTTCCTTGAATGTATTATC XP_011534499.1:n.1570+70_1570+71insCTTCCTTGAATGTATTATC
XM_011536198.1:c.1474+70_1474+71insCTTCCTTGAATGTATTATC XP_011534500.1:n.1474+70_1474+71insCTTCCTTGAATGTATTATC
XM_006715586.3:c.1474+70_1474+71insCTTCCTTGAATGTATTATC XP_006715649.1:n.1474+70_1474+71insCTTCCTTGAATGTATTATC
XM_011536196.3:c.1663+70_1663+71insCTTCCTTGAATGTATTATC XP_011534498.1:n.1663+70_1663+71insCTTCCTTGAATGTATTATC
XM_011536198.3:c.1474+70_1474+71insCTTCCTTGAATGTATTATC XP_011534500.1:n.1474+70_1474+71insCTTCCTTGAATGTATTATC
XM_024446573.1:c.1684+70_1684+71insCTTCCTTGAATGTATTATC XP_024302341.1:n.1684+70_1684+71insCTTCCTTGAATGTATTATC
XR_001743697.2:n.1715+70_1715+71insCTTCCTTGAATGTATTATC
XR_942606.2:n.1766+70_1766+71insCTTCCTTGAATGTATTATC
NM_032861.4:c.1684+70_1684+71insCTTCCTTGAATGTATTATC MANE Select NP_116250.3:n.1684+70_1684+71insCTTCCTTGAATGTATTATC
NR_073096.2:n.1669_1670insCTTCCTTGAATGTATTATC