Canonical Allele Identifier: CA1675959418
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114850T= , CM000668.2:g.158114850T= GRCh38
NC_000006.11:g.158535882T= , CM000668.1:g.158535882T= GRCh37
NC_000006.10:g.158455870T= NCBI36
NG_032889.1:g.58431A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.835A= ENSP00000391168.2:n.835A=
ENST00000607071.6:c.*1343A= ENSP00000475855.1:n.*1343A=
ENST00000642244.1:c.1533A= ENSP00000493554.1:p.Glu511=
ENST00000642903.1:c.1623A= ENSP00000493559.1:p.Glu541=
ENST00000644972.1:c.1623A= ENSP00000496451.1:p.Glu541=
ENST00000645077.1:c.*1244A= ENSP00000496113.1:n.*1244A=
ENST00000645172.1:c.*1325A= ENSP00000495367.1:n.*1325A=
ENST00000646190.1:n.2954A=
ENST00000646208.1:c.1359A= ENSP00000493723.1:p.Glu453=
ENST00000646410.1:c.1494A= ENSP00000494205.1:p.Glu498=
ENST00000646562.1:c.*1457A= ENSP00000496087.1:n.*1457A=
ENST00000647468.2:c.1623A= MANE Select ENSP00000496731.1:p.Glu541=
ENST00000648111.1:c.*1311A= ENSP00000497275.1:n.*1311A=
ENST00000367101.5:c.*71A= ENSP00000356068.1:n.*71A=
ENST00000367104.7:c.1623A= ENSP00000356071.3:p.Glu541=
ENST00000435180.5:c.348A= ENSP00000391168.1:p.Glu116=
ENST00000606965.5:c.*184A= ENSP00000475808.1:n.*184A=
ENST00000607071.5:c.*1557A= ENSP00000475855.1:n.*1557A=
ENST00000607742.5:c.*2901A= ENSP00000475523.1:n.*2901A=
NM_032861.3:c.1623A= NP_116250.3:p.Glu541=
NR_073096.1:n.1556A=
XM_006715586.1:c.1413A= XP_006715649.1:p.Glu471=
XM_011536196.1:c.1602A= XP_011534498.1:p.Glu534=
XM_011536197.1:c.1509A= XP_011534499.1:p.Glu503=
XM_011536198.1:c.1413A= XP_011534500.1:p.Glu471=
XM_006715586.3:c.1413A= XP_006715649.1:p.Glu471=
XM_011536196.3:c.1602A= XP_011534498.1:p.Glu534=
XM_011536198.3:c.1413A= XP_011534500.1:p.Glu471=
XM_024446573.1:c.1623A= XP_024302341.1:p.Glu541=
XR_001743697.2:n.1654A=
XR_942606.2:n.1705A=
NM_032861.4:c.1623A= MANE Select NP_116250.3:p.Glu541=
NR_073096.2:n.1538A=