Canonical Allele Identifier: CA2680956710
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114787_158114788insACAAGTATTA , CM000668.2:g.158114787_158114788insACAAGTATTA GRCh38
NC_000006.11:g.158535819_158535820insACAAGTATTA , CM000668.1:g.158535819_158535820insACAAGTATTA GRCh37
NC_000006.10:g.158455807_158455808insACAAGTATTA NCBI36
NG_032889.1:g.58501_58502insGTTAATACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1404+9_*1404+10insGTTAATACTT ENSP00000475855.1:n.*1404+9_*1404+10insGTTAATACTT
ENST00000642244.1:c.1594+9_1594+10insGTTAATACTT ENSP00000493554.1:n.1594+9_1594+10insGTTAATACTT
ENST00000642903.1:c.1693_1694insGTTAATACTT ENSP00000493559.1:p.Phe565CysfsTer2
ENST00000644972.1:c.1684+9_1684+10insGTTAATACTT ENSP00000496451.1:n.1684+9_1684+10insGTTAATACTT
ENST00000645077.1:c.*1305+9_*1305+10insGTTAATACTT ENSP00000496113.1:n.*1305+9_*1305+10insGTTAATACTT
ENST00000645172.1:c.*1386+9_*1386+10insGTTAATACTT ENSP00000495367.1:n.*1386+9_*1386+10insGTTAATACTT
ENST00000646190.1:n.3015+9_3015+10insGTTAATACTT
ENST00000646208.1:c.1420+9_1420+10insGTTAATACTT ENSP00000493723.1:n.1420+9_1420+10insGTTAATACTT
ENST00000646410.1:c.1555+9_1555+10insGTTAATACTT ENSP00000494205.1:n.1555+9_1555+10insGTTAATACTT
ENST00000646562.1:c.*1527_*1528insGTTAATACTT ENSP00000496087.1:n.*1527_*1528insGTTAATACTT
ENST00000647468.2:c.1684+9_1684+10insGTTAATACTT MANE Select ENSP00000496731.1:n.1684+9_1684+10insGTTAATACTT
ENST00000648111.1:c.*1372+9_*1372+10insGTTAATACTT ENSP00000497275.1:n.*1372+9_*1372+10insGTTAATACTT
ENST00000367101.5:c.*141_*142insGTTAATACTT ENSP00000356068.1:n.*141_*142insGTTAATACTT
ENST00000367104.7:c.1684+9_1684+10insGTTAATACTT ENSP00000356071.3:n.1684+9_1684+10insGTTAATACTT
ENST00000435180.5:c.418_419insGTTAATACTT ENSP00000391168.1:p.Phe140CysfsTer2
ENST00000606965.5:c.*254_*255insGTTAATACTT ENSP00000475808.1:n.*254_*255insGTTAATACTT
ENST00000607071.5:c.*1618+9_*1618+10insGTTAATACTT ENSP00000475855.1:n.*1618+9_*1618+10insGTTAATACTT
ENST00000607742.5:c.*2962+9_*2962+10insGTTAATACTT ENSP00000475523.1:n.*2962+9_*2962+10insGTTAATACTT
NM_032861.3:c.1684+9_1684+10insGTTAATACTT NP_116250.3:n.1684+9_1684+10insGTTAATACTT
NR_073096.1:n.1626_1627insGTTAATACTT
XM_006715586.1:c.1474+9_1474+10insGTTAATACTT XP_006715649.1:n.1474+9_1474+10insGTTAATACTT
XM_011536196.1:c.1663+9_1663+10insGTTAATACTT XP_011534498.1:n.1663+9_1663+10insGTTAATACTT
XM_011536197.1:c.1570+9_1570+10insGTTAATACTT XP_011534499.1:n.1570+9_1570+10insGTTAATACTT
XM_011536198.1:c.1474+9_1474+10insGTTAATACTT XP_011534500.1:n.1474+9_1474+10insGTTAATACTT
XM_006715586.3:c.1474+9_1474+10insGTTAATACTT XP_006715649.1:n.1474+9_1474+10insGTTAATACTT
XM_011536196.3:c.1663+9_1663+10insGTTAATACTT XP_011534498.1:n.1663+9_1663+10insGTTAATACTT
XM_011536198.3:c.1474+9_1474+10insGTTAATACTT XP_011534500.1:n.1474+9_1474+10insGTTAATACTT
XM_024446573.1:c.1684+9_1684+10insGTTAATACTT XP_024302341.1:n.1684+9_1684+10insGTTAATACTT
XR_001743697.2:n.1715+9_1715+10insGTTAATACTT
XR_942606.2:n.1766+9_1766+10insGTTAATACTT
NM_032861.4:c.1684+9_1684+10insGTTAATACTT MANE Select NP_116250.3:n.1684+9_1684+10insGTTAATACTT
NR_073096.2:n.1608_1609insGTTAATACTT