Canonical Allele Identifier: CA366264809
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158146878A>C , CM000668.2:g.158146878A>C GRCh38
NC_000006.11:g.158567910A>C , CM000668.1:g.158567910A>C GRCh37
NC_000006.10:g.158487898A>C NCBI36
NG_032889.1:g.26403T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*225T>G ENSP00000475855.1:n.*225T>G
ENST00000642244.1:c.301T>G ENSP00000493554.1:p.Cys101Gly
ENST00000642903.1:c.391T>G ENSP00000493559.1:p.Cys131Gly
ENST00000643093.1:n.441T>G
ENST00000644972.1:c.391T>G ENSP00000496451.1:p.Cys131Gly
ENST00000645077.1:c.*225T>G ENSP00000496113.1:n.*225T>G
ENST00000645172.1:c.*189+1987T>G ENSP00000495367.1:n.*189+1987T>G
ENST00000646190.1:n.1622T>G
ENST00000646208.1:c.127T>G ENSP00000493723.1:p.Cys43Gly
ENST00000646410.1:c.262T>G ENSP00000494205.1:p.Cys88Gly
ENST00000646562.1:c.*225T>G ENSP00000496087.1:n.*225T>G
ENST00000647468.2:c.391T>G MANE Select ENSP00000496731.1:p.Cys131Gly
ENST00000648111.1:c.*35T>G ENSP00000497275.1:n.*35T>G
ENST00000367101.5:c.391T>G ENSP00000356068.1:p.Cys131Gly
ENST00000367104.7:c.391T>G ENSP00000356071.3:p.Cys131Gly
ENST00000606965.5:c.391T>G ENSP00000475808.1:p.Cys131Gly
ENST00000607000.1:c.391T>G ENSP00000475788.1:p.Cys131Gly
ENST00000607071.5:c.*225T>G ENSP00000475855.1:n.*225T>G
ENST00000607742.5:c.*225T>G ENSP00000475523.1:n.*225T>G
NM_032861.3:c.391T>G NP_116250.3:p.Cys131Gly
NR_073096.1:n.533T>G
XM_006715586.1:c.181T>G XP_006715649.1:p.Cys61Gly
XM_011536196.1:c.370T>G XP_011534498.1:p.Cys124Gly
XM_011536197.1:c.391T>G XP_011534499.1:p.Cys131Gly
XM_011536198.1:c.181T>G XP_011534500.1:p.Cys61Gly
XR_942606.1:n.392T>G
XM_006715586.3:c.181T>G XP_006715649.1:p.Cys61Gly
XM_011536196.3:c.370T>G XP_011534498.1:p.Cys124Gly
XM_011536198.3:c.181T>G XP_011534500.1:p.Cys61Gly
XM_024446573.1:c.391T>G XP_024302341.1:p.Cys131Gly
XR_001743697.2:n.472T>G
XR_942606.2:n.523T>G
NM_032861.4:c.391T>G MANE Select NP_116250.3:p.Cys131Gly
NR_073096.2:n.515T>G