Canonical Allele Identifier: CA366255311
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114973T>C , CM000668.2:g.158114973T>C GRCh38
NC_000006.11:g.158536005T>C , CM000668.1:g.158536005T>C GRCh37
NC_000006.10:g.158455993T>C NCBI36
NG_032889.1:g.58308A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.714-2A>G ENSP00000391168.2:n.714-2A>G
ENST00000607071.6:c.*1222-2A>G ENSP00000475855.1:n.*1222-2A>G
ENST00000642244.1:c.1412-2A>G ENSP00000493554.1:n.1412-2A>G
ENST00000642903.1:c.1502-2A>G ENSP00000493559.1:n.1502-2A>G
ENST00000644972.1:c.1502-2A>G ENSP00000496451.1:n.1502-2A>G
ENST00000645077.1:c.*1123-2A>G ENSP00000496113.1:n.*1123-2A>G
ENST00000645172.1:c.*1204-2A>G ENSP00000495367.1:n.*1204-2A>G
ENST00000646190.1:n.2833-2A>G
ENST00000646208.1:c.1238-2A>G ENSP00000493723.1:n.1238-2A>G
ENST00000646410.1:c.1373-2A>G ENSP00000494205.1:n.1373-2A>G
ENST00000646562.1:c.*1336-2A>G ENSP00000496087.1:n.*1336-2A>G
ENST00000647468.2:c.1502-2A>G MANE Select ENSP00000496731.1:n.1502-2A>G
ENST00000648111.1:c.*1190-2A>G ENSP00000497275.1:n.*1190-2A>G
ENST00000367101.5:c.1546-2A>G ENSP00000356068.1:n.1546-2A>G
ENST00000367104.7:c.1502-2A>G ENSP00000356071.3:n.1502-2A>G
ENST00000435180.5:c.227-2A>G ENSP00000391168.1:n.227-2A>G
ENST00000606965.5:c.*63-2A>G ENSP00000475808.1:n.*63-2A>G
ENST00000607071.5:c.*1436-2A>G ENSP00000475855.1:n.*1436-2A>G
ENST00000607742.5:c.*2780-2A>G ENSP00000475523.1:n.*2780-2A>G
NM_032861.3:c.1502-2A>G NP_116250.3:n.1502-2A>G
NR_073096.1:n.1435-2A>G
XM_006715586.1:c.1292-2A>G XP_006715649.1:n.1292-2A>G
XM_011536196.1:c.1481-2A>G XP_011534498.1:n.1481-2A>G
XM_011536197.1:c.1388-2A>G XP_011534499.1:n.1388-2A>G
XM_011536198.1:c.1292-2A>G XP_011534500.1:n.1292-2A>G
XM_006715586.3:c.1292-2A>G XP_006715649.1:n.1292-2A>G
XM_011536196.3:c.1481-2A>G XP_011534498.1:n.1481-2A>G
XM_011536198.3:c.1292-2A>G XP_011534500.1:n.1292-2A>G
XM_024446573.1:c.1502-2A>G XP_024302341.1:n.1502-2A>G
XR_001743697.2:n.1533-2A>G
XR_942606.2:n.1584-2A>G
NM_032861.4:c.1502-2A>G MANE Select NP_116250.3:n.1502-2A>G
NR_073096.2:n.1417-2A>G