Canonical Allele Identifier: CA1675959493
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114948A= , CM000668.2:g.158114948A= GRCh38
NC_000006.11:g.158535980A= , CM000668.1:g.158535980A= GRCh37
NC_000006.10:g.158455968A= NCBI36
NG_032889.1:g.58333T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.737T= ENSP00000391168.2:n.737T=
ENST00000607071.6:c.*1245T= ENSP00000475855.1:n.*1245T=
ENST00000642244.1:c.1435T= ENSP00000493554.1:p.Leu479=
ENST00000642903.1:c.1525T= ENSP00000493559.1:p.Leu509=
ENST00000644972.1:c.1525T= ENSP00000496451.1:p.Leu509=
ENST00000645077.1:c.*1146T= ENSP00000496113.1:n.*1146T=
ENST00000645172.1:c.*1227T= ENSP00000495367.1:n.*1227T=
ENST00000646190.1:n.2856T=
ENST00000646208.1:c.1261T= ENSP00000493723.1:p.Leu421=
ENST00000646410.1:c.1396T= ENSP00000494205.1:p.Leu466=
ENST00000646562.1:c.*1359T= ENSP00000496087.1:n.*1359T=
ENST00000647468.2:c.1525T= MANE Select ENSP00000496731.1:p.Leu509=
ENST00000648111.1:c.*1213T= ENSP00000497275.1:n.*1213T=
ENST00000367101.5:c.1569T= ENSP00000356068.1:p.Cys523=
ENST00000367104.7:c.1525T= ENSP00000356071.3:p.Leu509=
ENST00000435180.5:c.250T= ENSP00000391168.1:p.Leu84=
ENST00000606965.5:c.*86T= ENSP00000475808.1:n.*86T=
ENST00000607071.5:c.*1459T= ENSP00000475855.1:n.*1459T=
ENST00000607742.5:c.*2803T= ENSP00000475523.1:n.*2803T=
NM_032861.3:c.1525T= NP_116250.3:p.Leu509=
NR_073096.1:n.1458T=
XM_006715586.1:c.1315T= XP_006715649.1:p.Leu439=
XM_011536196.1:c.1504T= XP_011534498.1:p.Leu502=
XM_011536197.1:c.1411T= XP_011534499.1:p.Leu471=
XM_011536198.1:c.1315T= XP_011534500.1:p.Leu439=
XM_006715586.3:c.1315T= XP_006715649.1:p.Leu439=
XM_011536196.3:c.1504T= XP_011534498.1:p.Leu502=
XM_011536198.3:c.1315T= XP_011534500.1:p.Leu439=
XM_024446573.1:c.1525T= XP_024302341.1:p.Leu509=
XR_001743697.2:n.1556T=
XR_942606.2:n.1607T=
NM_032861.4:c.1525T= MANE Select NP_116250.3:p.Leu509=
NR_073096.2:n.1440T=