Canonical Allele Identifier: CA1675959365
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114816A= , CM000668.2:g.158114816A= GRCh38
NC_000006.11:g.158535848A= , CM000668.1:g.158535848A= GRCh37
NC_000006.10:g.158455836A= NCBI36
NG_032889.1:g.58465T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1377T= ENSP00000475855.1:n.*1377T=
ENST00000642244.1:c.1567T= ENSP00000493554.1:p.Ser523=
ENST00000642903.1:c.1657T= ENSP00000493559.1:p.Ser553=
ENST00000644972.1:c.1657T= ENSP00000496451.1:p.Ser553=
ENST00000645077.1:c.*1278T= ENSP00000496113.1:n.*1278T=
ENST00000645172.1:c.*1359T= ENSP00000495367.1:n.*1359T=
ENST00000646190.1:n.2988T=
ENST00000646208.1:c.1393T= ENSP00000493723.1:p.Ser465=
ENST00000646410.1:c.1528T= ENSP00000494205.1:p.Ser510=
ENST00000646562.1:c.*1491T= ENSP00000496087.1:n.*1491T=
ENST00000647468.2:c.1657T= MANE Select ENSP00000496731.1:p.Ser553=
ENST00000648111.1:c.*1345T= ENSP00000497275.1:n.*1345T=
ENST00000367101.5:c.*105T= ENSP00000356068.1:n.*105T=
ENST00000367104.7:c.1657T= ENSP00000356071.3:p.Ser553=
ENST00000435180.5:c.382T= ENSP00000391168.1:p.Ser128=
ENST00000606965.5:c.*218T= ENSP00000475808.1:n.*218T=
ENST00000607071.5:c.*1591T= ENSP00000475855.1:n.*1591T=
ENST00000607742.5:c.*2935T= ENSP00000475523.1:n.*2935T=
NM_032861.3:c.1657T= NP_116250.3:p.Ser553=
NR_073096.1:n.1590T=
XM_006715586.1:c.1447T= XP_006715649.1:p.Ser483=
XM_011536196.1:c.1636T= XP_011534498.1:p.Ser546=
XM_011536197.1:c.1543T= XP_011534499.1:p.Ser515=
XM_011536198.1:c.1447T= XP_011534500.1:p.Ser483=
XM_006715586.3:c.1447T= XP_006715649.1:p.Ser483=
XM_011536196.3:c.1636T= XP_011534498.1:p.Ser546=
XM_011536198.3:c.1447T= XP_011534500.1:p.Ser483=
XM_024446573.1:c.1657T= XP_024302341.1:p.Ser553=
XR_001743697.2:n.1688T=
XR_942606.2:n.1739T=
NM_032861.4:c.1657T= MANE Select NP_116250.3:p.Ser553=
NR_073096.2:n.1572T=