Canonical Allele Identifier: CA1675955848
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158146905T= , CM000668.2:g.158146905T= GRCh38
NC_000006.11:g.158567937T= , CM000668.1:g.158567937T= GRCh37
NC_000006.10:g.158487925T= NCBI36
NG_032889.1:g.26376A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*198A= ENSP00000475855.1:n.*198A=
ENST00000642244.1:c.274A= ENSP00000493554.1:p.Ser92=
ENST00000642903.1:c.364A= ENSP00000493559.1:p.Ser122=
ENST00000643093.1:n.414A=
ENST00000644972.1:c.364A= ENSP00000496451.1:p.Ser122=
ENST00000645077.1:c.*198A= ENSP00000496113.1:n.*198A=
ENST00000645172.1:c.*189+1960A= ENSP00000495367.1:n.*189+1960A=
ENST00000646190.1:n.1595A=
ENST00000646208.1:c.100A= ENSP00000493723.1:p.Ser34=
ENST00000646410.1:c.235A= ENSP00000494205.1:p.Ser79=
ENST00000646562.1:c.*198A= ENSP00000496087.1:n.*198A=
ENST00000647468.2:c.364A= MANE Select ENSP00000496731.1:p.Ser122=
ENST00000648111.1:c.*8A= ENSP00000497275.1:n.*8A=
ENST00000367101.5:c.364A= ENSP00000356068.1:p.Ser122=
ENST00000367104.7:c.364A= ENSP00000356071.3:p.Ser122=
ENST00000606965.5:c.364A= ENSP00000475808.1:p.Ser122=
ENST00000607000.1:c.364A= ENSP00000475788.1:p.Ser122=
ENST00000607071.5:c.*198A= ENSP00000475855.1:n.*198A=
ENST00000607742.5:c.*198A= ENSP00000475523.1:n.*198A=
NM_032861.3:c.364A= NP_116250.3:p.Ser122=
NR_073096.1:n.506A=
XM_006715586.1:c.154A= XP_006715649.1:p.Ser52=
XM_011536196.1:c.343A= XP_011534498.1:p.Ser115=
XM_011536197.1:c.364A= XP_011534499.1:p.Ser122=
XM_011536198.1:c.154A= XP_011534500.1:p.Ser52=
XR_942606.1:n.365A=
XM_006715586.3:c.154A= XP_006715649.1:p.Ser52=
XM_011536196.3:c.343A= XP_011534498.1:p.Ser115=
XM_011536198.3:c.154A= XP_011534500.1:p.Ser52=
XM_024446573.1:c.364A= XP_024302341.1:p.Ser122=
XR_001743697.2:n.445A=
XR_942606.2:n.496A=
NM_032861.4:c.364A= MANE Select NP_116250.3:p.Ser122=
NR_073096.2:n.488A=