Canonical Allele Identifier: CA366255197
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114931C>G , CM000668.2:g.158114931C>G GRCh38
NC_000006.11:g.158535963C>G , CM000668.1:g.158535963C>G GRCh37
NC_000006.10:g.158455951C>G NCBI36
NG_032889.1:g.58350G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.754G>C ENSP00000391168.2:n.754G>C
ENST00000607071.6:c.*1262G>C ENSP00000475855.1:n.*1262G>C
ENST00000642244.1:c.1452G>C ENSP00000493554.1:p.Lys484Asn
ENST00000642903.1:c.1542G>C ENSP00000493559.1:p.Lys514Asn
ENST00000644972.1:c.1542G>C ENSP00000496451.1:p.Lys514Asn
ENST00000645077.1:c.*1163G>C ENSP00000496113.1:n.*1163G>C
ENST00000645172.1:c.*1244G>C ENSP00000495367.1:n.*1244G>C
ENST00000646190.1:n.2873G>C
ENST00000646208.1:c.1278G>C ENSP00000493723.1:p.Lys426Asn
ENST00000646410.1:c.1413G>C ENSP00000494205.1:p.Lys471Asn
ENST00000646562.1:c.*1376G>C ENSP00000496087.1:n.*1376G>C
ENST00000647468.2:c.1542G>C MANE Select ENSP00000496731.1:p.Lys514Asn
ENST00000648111.1:c.*1230G>C ENSP00000497275.1:n.*1230G>C
ENST00000367101.5:c.1586G>C ENSP00000356068.1:p.Ser529Thr
ENST00000367104.7:c.1542G>C ENSP00000356071.3:p.Lys514Asn
ENST00000435180.5:c.267G>C ENSP00000391168.1:p.Lys89Asn
ENST00000606965.5:c.*103G>C ENSP00000475808.1:n.*103G>C
ENST00000607071.5:c.*1476G>C ENSP00000475855.1:n.*1476G>C
ENST00000607742.5:c.*2820G>C ENSP00000475523.1:n.*2820G>C
NM_032861.3:c.1542G>C NP_116250.3:p.Lys514Asn
NR_073096.1:n.1475G>C
XM_006715586.1:c.1332G>C XP_006715649.1:p.Lys444Asn
XM_011536196.1:c.1521G>C XP_011534498.1:p.Lys507Asn
XM_011536197.1:c.1428G>C XP_011534499.1:p.Lys476Asn
XM_011536198.1:c.1332G>C XP_011534500.1:p.Lys444Asn
XM_006715586.3:c.1332G>C XP_006715649.1:p.Lys444Asn
XM_011536196.3:c.1521G>C XP_011534498.1:p.Lys507Asn
XM_011536198.3:c.1332G>C XP_011534500.1:p.Lys444Asn
XM_024446573.1:c.1542G>C XP_024302341.1:p.Lys514Asn
XR_001743697.2:n.1573G>C
XR_942606.2:n.1624G>C
NM_032861.4:c.1542G>C MANE Select NP_116250.3:p.Lys514Asn
NR_073096.2:n.1457G>C