Canonical Allele Identifier: CA366255135
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114906T>A , CM000668.2:g.158114906T>A GRCh38
NC_000006.11:g.158535938T>A , CM000668.1:g.158535938T>A GRCh37
NC_000006.10:g.158455926T>A NCBI36
NG_032889.1:g.58375A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.779A>T ENSP00000391168.2:n.779A>T
ENST00000607071.6:c.*1287A>T ENSP00000475855.1:n.*1287A>T
ENST00000642244.1:c.1477A>T ENSP00000493554.1:p.Asn493Tyr
ENST00000642903.1:c.1567A>T ENSP00000493559.1:p.Asn523Tyr
ENST00000644972.1:c.1567A>T ENSP00000496451.1:p.Asn523Tyr
ENST00000645077.1:c.*1188A>T ENSP00000496113.1:n.*1188A>T
ENST00000645172.1:c.*1269A>T ENSP00000495367.1:n.*1269A>T
ENST00000646190.1:n.2898A>T
ENST00000646208.1:c.1303A>T ENSP00000493723.1:p.Asn435Tyr
ENST00000646410.1:c.1438A>T ENSP00000494205.1:p.Asn480Tyr
ENST00000646562.1:c.*1401A>T ENSP00000496087.1:n.*1401A>T
ENST00000647468.2:c.1567A>T MANE Select ENSP00000496731.1:p.Asn523Tyr
ENST00000648111.1:c.*1255A>T ENSP00000497275.1:n.*1255A>T
ENST00000367101.5:c.*15A>T ENSP00000356068.1:n.*15A>T
ENST00000367104.7:c.1567A>T ENSP00000356071.3:p.Asn523Tyr
ENST00000435180.5:c.292A>T ENSP00000391168.1:p.Asn98Tyr
ENST00000606965.5:c.*128A>T ENSP00000475808.1:n.*128A>T
ENST00000607071.5:c.*1501A>T ENSP00000475855.1:n.*1501A>T
ENST00000607742.5:c.*2845A>T ENSP00000475523.1:n.*2845A>T
NM_032861.3:c.1567A>T NP_116250.3:p.Asn523Tyr
NR_073096.1:n.1500A>T
XM_006715586.1:c.1357A>T XP_006715649.1:p.Asn453Tyr
XM_011536196.1:c.1546A>T XP_011534498.1:p.Asn516Tyr
XM_011536197.1:c.1453A>T XP_011534499.1:p.Asn485Tyr
XM_011536198.1:c.1357A>T XP_011534500.1:p.Asn453Tyr
XM_006715586.3:c.1357A>T XP_006715649.1:p.Asn453Tyr
XM_011536196.3:c.1546A>T XP_011534498.1:p.Asn516Tyr
XM_011536198.3:c.1357A>T XP_011534500.1:p.Asn453Tyr
XM_024446573.1:c.1567A>T XP_024302341.1:p.Asn523Tyr
XR_001743697.2:n.1598A>T
XR_942606.2:n.1649A>T
NM_032861.4:c.1567A>T MANE Select NP_116250.3:p.Asn523Tyr
NR_073096.2:n.1482A>T