Canonical Allele Identifier: CA366255296
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114967A>T , CM000668.2:g.158114967A>T GRCh38
NC_000006.11:g.158535999A>T , CM000668.1:g.158535999A>T GRCh37
NC_000006.10:g.158455987A>T NCBI36
NG_032889.1:g.58314T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.718T>A ENSP00000391168.2:n.718T>A
ENST00000607071.6:c.*1226T>A ENSP00000475855.1:n.*1226T>A
ENST00000642244.1:c.1416T>A ENSP00000493554.1:p.Leu472=
ENST00000642903.1:c.1506T>A ENSP00000493559.1:p.Leu502=
ENST00000644972.1:c.1506T>A ENSP00000496451.1:p.Leu502=
ENST00000645077.1:c.*1127T>A ENSP00000496113.1:n.*1127T>A
ENST00000645172.1:c.*1208T>A ENSP00000495367.1:n.*1208T>A
ENST00000646190.1:n.2837T>A
ENST00000646208.1:c.1242T>A ENSP00000493723.1:p.Leu414=
ENST00000646410.1:c.1377T>A ENSP00000494205.1:p.Leu459=
ENST00000646562.1:c.*1340T>A ENSP00000496087.1:n.*1340T>A
ENST00000647468.2:c.1506T>A MANE Select ENSP00000496731.1:p.Leu502=
ENST00000648111.1:c.*1194T>A ENSP00000497275.1:n.*1194T>A
ENST00000367101.5:c.1550T>A ENSP00000356068.1:p.Phe517Tyr
ENST00000367104.7:c.1506T>A ENSP00000356071.3:p.Leu502=
ENST00000435180.5:c.231T>A ENSP00000391168.1:p.Leu77=
ENST00000606965.5:c.*67T>A ENSP00000475808.1:n.*67T>A
ENST00000607071.5:c.*1440T>A ENSP00000475855.1:n.*1440T>A
ENST00000607742.5:c.*2784T>A ENSP00000475523.1:n.*2784T>A
NM_032861.3:c.1506T>A NP_116250.3:p.Leu502=
NR_073096.1:n.1439T>A
XM_006715586.1:c.1296T>A XP_006715649.1:p.Leu432=
XM_011536196.1:c.1485T>A XP_011534498.1:p.Leu495=
XM_011536197.1:c.1392T>A XP_011534499.1:p.Leu464=
XM_011536198.1:c.1296T>A XP_011534500.1:p.Leu432=
XM_006715586.3:c.1296T>A XP_006715649.1:p.Leu432=
XM_011536196.3:c.1485T>A XP_011534498.1:p.Leu495=
XM_011536198.3:c.1296T>A XP_011534500.1:p.Leu432=
XM_024446573.1:c.1506T>A XP_024302341.1:p.Leu502=
XR_001743697.2:n.1537T>A
XR_942606.2:n.1588T>A
NM_032861.4:c.1506T>A MANE Select NP_116250.3:p.Leu502=
NR_073096.2:n.1421T>A