Canonical Allele Identifier: CA1675959261
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114750_158114751delinsTA , CM000668.2:g.158114750_158114751delinsTA GRCh38
NC_000006.11:g.158535782_158535783delinsTA , CM000668.1:g.158535782_158535783delinsTA GRCh37
NC_000006.10:g.158455770_158455771delinsTA NCBI36
NG_032889.1:g.58530_58531delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1404+38_*1404+39delinsTA ENSP00000475855.1:n.*1404+38_*1404+39delinsTA
ENST00000642244.1:c.1594+38_1594+39delinsTA ENSP00000493554.1:n.1594+38_1594+39delinsTA
ENST00000642903.1:c.1722_1723delinsTA ENSP00000493559.1:p.Ile574=
ENST00000644972.1:c.1684+38_1684+39delinsTA ENSP00000496451.1:n.1684+38_1684+39delinsTA
ENST00000645077.1:c.*1305+38_*1305+39delinsTA ENSP00000496113.1:n.*1305+38_*1305+39delinsTA
ENST00000645172.1:c.*1386+38_*1386+39delinsTA ENSP00000495367.1:n.*1386+38_*1386+39delinsTA
ENST00000646190.1:n.3015+38_3015+39delinsTA
ENST00000646208.1:c.1420+38_1420+39delinsTA ENSP00000493723.1:n.1420+38_1420+39delinsTA
ENST00000646410.1:c.1555+38_1555+39delinsTA ENSP00000494205.1:n.1555+38_1555+39delinsTA
ENST00000646562.1:c.*1556_*1557delinsTA ENSP00000496087.1:n.*1556_*1557delinsTA
ENST00000647468.2:c.1684+38_1684+39delinsTA MANE Select ENSP00000496731.1:n.1684+38_1684+39delinsTA
ENST00000648111.1:c.*1372+38_*1372+39delinsTA ENSP00000497275.1:n.*1372+38_*1372+39delinsTA
ENST00000367101.5:c.*170_*171delinsTA ENSP00000356068.1:n.*170_*171delinsTA
ENST00000367104.7:c.1684+38_1684+39delinsTA ENSP00000356071.3:n.1684+38_1684+39delinsTA
ENST00000435180.5:c.447_448delinsTA ENSP00000391168.1:p.Ile149=
ENST00000606965.5:c.*283_*284delinsTA ENSP00000475808.1:n.*283_*284delinsTA
ENST00000607071.5:c.*1618+38_*1618+39delinsTA ENSP00000475855.1:n.*1618+38_*1618+39delinsTA
ENST00000607742.5:c.*2962+38_*2962+39delinsTA ENSP00000475523.1:n.*2962+38_*2962+39delinsTA
NM_032861.3:c.1684+38_1684+39delinsTA NP_116250.3:n.1684+38_1684+39delinsTA
NR_073096.1:n.1655_1656delinsTA
XM_006715586.1:c.1474+38_1474+39delinsTA XP_006715649.1:n.1474+38_1474+39delinsTA
XM_011536196.1:c.1663+38_1663+39delinsTA XP_011534498.1:n.1663+38_1663+39delinsTA
XM_011536197.1:c.1570+38_1570+39delinsTA XP_011534499.1:n.1570+38_1570+39delinsTA
XM_011536198.1:c.1474+38_1474+39delinsTA XP_011534500.1:n.1474+38_1474+39delinsTA
XM_006715586.3:c.1474+38_1474+39delinsTA XP_006715649.1:n.1474+38_1474+39delinsTA
XM_011536196.3:c.1663+38_1663+39delinsTA XP_011534498.1:n.1663+38_1663+39delinsTA
XM_011536198.3:c.1474+38_1474+39delinsTA XP_011534500.1:n.1474+38_1474+39delinsTA
XM_024446573.1:c.1684+38_1684+39delinsTA XP_024302341.1:n.1684+38_1684+39delinsTA
XR_001743697.2:n.1715+38_1715+39delinsTA
XR_942606.2:n.1766+38_1766+39delinsTA
NM_032861.4:c.1684+38_1684+39delinsTA MANE Select NP_116250.3:n.1684+38_1684+39delinsTA
NR_073096.2:n.1637_1638delinsTA