Canonical Allele Identifier: CA366255067
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114878A>C , CM000668.2:g.158114878A>C GRCh38
NC_000006.11:g.158535910A>C , CM000668.1:g.158535910A>C GRCh37
NC_000006.10:g.158455898A>C NCBI36
NG_032889.1:g.58403T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.807T>G ENSP00000391168.2:n.807T>G
ENST00000607071.6:c.*1315T>G ENSP00000475855.1:n.*1315T>G
ENST00000642244.1:c.1505T>G ENSP00000493554.1:p.Val502Gly
ENST00000642903.1:c.1595T>G ENSP00000493559.1:p.Val532Gly
ENST00000644972.1:c.1595T>G ENSP00000496451.1:p.Val532Gly
ENST00000645077.1:c.*1216T>G ENSP00000496113.1:n.*1216T>G
ENST00000645172.1:c.*1297T>G ENSP00000495367.1:n.*1297T>G
ENST00000646190.1:n.2926T>G
ENST00000646208.1:c.1331T>G ENSP00000493723.1:p.Val444Gly
ENST00000646410.1:c.1466T>G ENSP00000494205.1:p.Val489Gly
ENST00000646562.1:c.*1429T>G ENSP00000496087.1:n.*1429T>G
ENST00000647468.2:c.1595T>G MANE Select ENSP00000496731.1:p.Val532Gly
ENST00000648111.1:c.*1283T>G ENSP00000497275.1:n.*1283T>G
ENST00000367101.5:c.*43T>G ENSP00000356068.1:n.*43T>G
ENST00000367104.7:c.1595T>G ENSP00000356071.3:p.Val532Gly
ENST00000435180.5:c.320T>G ENSP00000391168.1:p.Val107Gly
ENST00000606965.5:c.*156T>G ENSP00000475808.1:n.*156T>G
ENST00000607071.5:c.*1529T>G ENSP00000475855.1:n.*1529T>G
ENST00000607742.5:c.*2873T>G ENSP00000475523.1:n.*2873T>G
NM_032861.3:c.1595T>G NP_116250.3:p.Val532Gly
NR_073096.1:n.1528T>G
XM_006715586.1:c.1385T>G XP_006715649.1:p.Val462Gly
XM_011536196.1:c.1574T>G XP_011534498.1:p.Val525Gly
XM_011536197.1:c.1481T>G XP_011534499.1:p.Val494Gly
XM_011536198.1:c.1385T>G XP_011534500.1:p.Val462Gly
XM_006715586.3:c.1385T>G XP_006715649.1:p.Val462Gly
XM_011536196.3:c.1574T>G XP_011534498.1:p.Val525Gly
XM_011536198.3:c.1385T>G XP_011534500.1:p.Val462Gly
XM_024446573.1:c.1595T>G XP_024302341.1:p.Val532Gly
XR_001743697.2:n.1626T>G
XR_942606.2:n.1677T>G
NM_032861.4:c.1595T>G MANE Select NP_116250.3:p.Val532Gly
NR_073096.2:n.1510T>G