Canonical Allele Identifier: CA366254991
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114840T>C , CM000668.2:g.158114840T>C GRCh38
NC_000006.11:g.158535872T>C , CM000668.1:g.158535872T>C GRCh37
NC_000006.10:g.158455860T>C NCBI36
NG_032889.1:g.58441A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.845A>G ENSP00000391168.2:n.845A>G
ENST00000607071.6:c.*1353A>G ENSP00000475855.1:n.*1353A>G
ENST00000642244.1:c.1543A>G ENSP00000493554.1:p.Asn515Asp
ENST00000642903.1:c.1633A>G ENSP00000493559.1:p.Asn545Asp
ENST00000644972.1:c.1633A>G ENSP00000496451.1:p.Asn545Asp
ENST00000645077.1:c.*1254A>G ENSP00000496113.1:n.*1254A>G
ENST00000645172.1:c.*1335A>G ENSP00000495367.1:n.*1335A>G
ENST00000646190.1:n.2964A>G
ENST00000646208.1:c.1369A>G ENSP00000493723.1:p.Asn457Asp
ENST00000646410.1:c.1504A>G ENSP00000494205.1:p.Asn502Asp
ENST00000646562.1:c.*1467A>G ENSP00000496087.1:n.*1467A>G
ENST00000647468.2:c.1633A>G MANE Select ENSP00000496731.1:p.Asn545Asp
ENST00000648111.1:c.*1321A>G ENSP00000497275.1:n.*1321A>G
ENST00000367101.5:c.*81A>G ENSP00000356068.1:n.*81A>G
ENST00000367104.7:c.1633A>G ENSP00000356071.3:p.Asn545Asp
ENST00000435180.5:c.358A>G ENSP00000391168.1:p.Asn120Asp
ENST00000606965.5:c.*194A>G ENSP00000475808.1:n.*194A>G
ENST00000607071.5:c.*1567A>G ENSP00000475855.1:n.*1567A>G
ENST00000607742.5:c.*2911A>G ENSP00000475523.1:n.*2911A>G
NM_032861.3:c.1633A>G NP_116250.3:p.Asn545Asp
NR_073096.1:n.1566A>G
XM_006715586.1:c.1423A>G XP_006715649.1:p.Asn475Asp
XM_011536196.1:c.1612A>G XP_011534498.1:p.Asn538Asp
XM_011536197.1:c.1519A>G XP_011534499.1:p.Asn507Asp
XM_011536198.1:c.1423A>G XP_011534500.1:p.Asn475Asp
XM_006715586.3:c.1423A>G XP_006715649.1:p.Asn475Asp
XM_011536196.3:c.1612A>G XP_011534498.1:p.Asn538Asp
XM_011536198.3:c.1423A>G XP_011534500.1:p.Asn475Asp
XM_024446573.1:c.1633A>G XP_024302341.1:p.Asn545Asp
XR_001743697.2:n.1664A>G
XR_942606.2:n.1715A>G
NM_032861.4:c.1633A>G MANE Select NP_116250.3:p.Asn545Asp
NR_073096.2:n.1548A>G