Canonical Allele Identifier: CA1675959062
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114615T= , CM000668.2:g.158114615T= GRCh38
NC_000006.11:g.158535647T= , CM000668.1:g.158535647T= GRCh37
NC_000006.10:g.158455635T= NCBI36
NG_032889.1:g.58666A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1404+174A= ENSP00000475855.1:n.*1404+174A=
ENST00000642244.1:c.1594+174A= ENSP00000493554.1:n.1594+174A=
ENST00000642903.1:c.*94A= ENSP00000493559.1:n.*94A=
ENST00000644972.1:c.1684+174A= ENSP00000496451.1:n.1684+174A=
ENST00000645077.1:c.*1305+174A= ENSP00000496113.1:n.*1305+174A=
ENST00000645172.1:c.*1386+174A= ENSP00000495367.1:n.*1386+174A=
ENST00000646190.1:n.3015+174A=
ENST00000646208.1:c.1420+174A= ENSP00000493723.1:n.1420+174A=
ENST00000646410.1:c.1555+174A= ENSP00000494205.1:n.1555+174A=
ENST00000646562.1:c.*1692A= ENSP00000496087.1:n.*1692A=
ENST00000647468.2:c.1684+174A= MANE Select ENSP00000496731.1:n.1684+174A=
ENST00000648111.1:c.*1372+174A= ENSP00000497275.1:n.*1372+174A=
ENST00000367104.7:c.1684+174A= ENSP00000356071.3:n.1684+174A=
ENST00000606965.5:c.*419A= ENSP00000475808.1:n.*419A=
ENST00000607071.5:c.*1618+174A= ENSP00000475855.1:n.*1618+174A=
ENST00000607742.5:c.*2962+174A= ENSP00000475523.1:n.*2962+174A=
NM_032861.3:c.1684+174A= NP_116250.3:n.1684+174A=
NR_073096.1:n.1791A=
XM_006715586.1:c.1474+174A= XP_006715649.1:n.1474+174A=
XM_011536196.1:c.1663+174A= XP_011534498.1:n.1663+174A=
XM_011536197.1:c.1570+174A= XP_011534499.1:n.1570+174A=
XM_011536198.1:c.1474+174A= XP_011534500.1:n.1474+174A=
XM_006715586.3:c.1474+174A= XP_006715649.1:n.1474+174A=
XM_011536196.3:c.1663+174A= XP_011534498.1:n.1663+174A=
XM_011536198.3:c.1474+174A= XP_011534500.1:n.1474+174A=
XM_024446573.1:c.1684+174A= XP_024302341.1:n.1684+174A=
XR_001743697.2:n.1715+174A=
XR_942606.2:n.1766+174A=
NM_032861.4:c.1684+174A= MANE Select NP_116250.3:n.1684+174A=
NR_073096.2:n.1773A=