Canonical Allele Identifier: CA366254924
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114809T>A , CM000668.2:g.158114809T>A GRCh38
NC_000006.11:g.158535841T>A , CM000668.1:g.158535841T>A GRCh37
NC_000006.10:g.158455829T>A NCBI36
NG_032889.1:g.58472A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1384A>T ENSP00000475855.1:n.*1384A>T
ENST00000642244.1:c.1574A>T ENSP00000493554.1:p.Glu525Val
ENST00000642903.1:c.1664A>T ENSP00000493559.1:p.Glu555Val
ENST00000644972.1:c.1664A>T ENSP00000496451.1:p.Glu555Val
ENST00000645077.1:c.*1285A>T ENSP00000496113.1:n.*1285A>T
ENST00000645172.1:c.*1366A>T ENSP00000495367.1:n.*1366A>T
ENST00000646190.1:n.2995A>T
ENST00000646208.1:c.1400A>T ENSP00000493723.1:p.Glu467Val
ENST00000646410.1:c.1535A>T ENSP00000494205.1:p.Glu512Val
ENST00000646562.1:c.*1498A>T ENSP00000496087.1:n.*1498A>T
ENST00000647468.2:c.1664A>T MANE Select ENSP00000496731.1:p.Glu555Val
ENST00000648111.1:c.*1352A>T ENSP00000497275.1:n.*1352A>T
ENST00000367101.5:c.*112A>T ENSP00000356068.1:n.*112A>T
ENST00000367104.7:c.1664A>T ENSP00000356071.3:p.Glu555Val
ENST00000435180.5:c.389A>T ENSP00000391168.1:p.Glu130Val
ENST00000606965.5:c.*225A>T ENSP00000475808.1:n.*225A>T
ENST00000607071.5:c.*1598A>T ENSP00000475855.1:n.*1598A>T
ENST00000607742.5:c.*2942A>T ENSP00000475523.1:n.*2942A>T
NM_032861.3:c.1664A>T NP_116250.3:p.Glu555Val
NR_073096.1:n.1597A>T
XM_006715586.1:c.1454A>T XP_006715649.1:p.Glu485Val
XM_011536196.1:c.1643A>T XP_011534498.1:p.Glu548Val
XM_011536197.1:c.1550A>T XP_011534499.1:p.Glu517Val
XM_011536198.1:c.1454A>T XP_011534500.1:p.Glu485Val
XM_006715586.3:c.1454A>T XP_006715649.1:p.Glu485Val
XM_011536196.3:c.1643A>T XP_011534498.1:p.Glu548Val
XM_011536198.3:c.1454A>T XP_011534500.1:p.Glu485Val
XM_024446573.1:c.1664A>T XP_024302341.1:p.Glu555Val
XR_001743697.2:n.1695A>T
XR_942606.2:n.1746A>T
NM_032861.4:c.1664A>T MANE Select NP_116250.3:p.Glu555Val
NR_073096.2:n.1579A>T