Canonical Allele Identifier: CA1675959490
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114941G= , CM000668.2:g.158114941G= GRCh38
NC_000006.11:g.158535973G= , CM000668.1:g.158535973G= GRCh37
NC_000006.10:g.158455961G= NCBI36
NG_032889.1:g.58340C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.744C= ENSP00000391168.2:n.744C=
ENST00000607071.6:c.*1252C= ENSP00000475855.1:n.*1252C=
ENST00000642244.1:c.1442C= ENSP00000493554.1:p.Ala481=
ENST00000642903.1:c.1532C= ENSP00000493559.1:p.Ala511=
ENST00000644972.1:c.1532C= ENSP00000496451.1:p.Ala511=
ENST00000645077.1:c.*1153C= ENSP00000496113.1:n.*1153C=
ENST00000645172.1:c.*1234C= ENSP00000495367.1:n.*1234C=
ENST00000646190.1:n.2863C=
ENST00000646208.1:c.1268C= ENSP00000493723.1:p.Ala423=
ENST00000646410.1:c.1403C= ENSP00000494205.1:p.Ala468=
ENST00000646562.1:c.*1366C= ENSP00000496087.1:n.*1366C=
ENST00000647468.2:c.1532C= MANE Select ENSP00000496731.1:p.Ala511=
ENST00000648111.1:c.*1220C= ENSP00000497275.1:n.*1220C=
ENST00000367101.5:c.1576C= ENSP00000356068.1:p.Pro526=
ENST00000367104.7:c.1532C= ENSP00000356071.3:p.Ala511=
ENST00000435180.5:c.257C= ENSP00000391168.1:p.Ala86=
ENST00000606965.5:c.*93C= ENSP00000475808.1:n.*93C=
ENST00000607071.5:c.*1466C= ENSP00000475855.1:n.*1466C=
ENST00000607742.5:c.*2810C= ENSP00000475523.1:n.*2810C=
NM_032861.3:c.1532C= NP_116250.3:p.Ala511=
NR_073096.1:n.1465C=
XM_006715586.1:c.1322C= XP_006715649.1:p.Ala441=
XM_011536196.1:c.1511C= XP_011534498.1:p.Ala504=
XM_011536197.1:c.1418C= XP_011534499.1:p.Ala473=
XM_011536198.1:c.1322C= XP_011534500.1:p.Ala441=
XM_006715586.3:c.1322C= XP_006715649.1:p.Ala441=
XM_011536196.3:c.1511C= XP_011534498.1:p.Ala504=
XM_011536198.3:c.1322C= XP_011534500.1:p.Ala441=
XM_024446573.1:c.1532C= XP_024302341.1:p.Ala511=
XR_001743697.2:n.1563C=
XR_942606.2:n.1614C=
NM_032861.4:c.1532C= MANE Select NP_116250.3:p.Ala511=
NR_073096.2:n.1447C=