Canonical Allele Identifier: CA1307408206
Gene: CYBRD1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.171554664_171554670delinsCCATTCT , CM000664.2:g.171554664_171554670delinsCCATTCT GRCh38
NC_000002.11:g.172411174_172411180delinsCCATTCT , CM000664.1:g.172411174_172411180delinsCCATTCT GRCh37
NC_000002.10:g.172119420_172119426delinsCCATTCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321348.9:c.698_704delinsCCATTCT MANE Select ENSP00000319141.4:p.Thr233=
ENST00000321348.8:c.698_704delinsCCATTCT ENSP00000319141.4:p.Thr233=
ENST00000375252.3:c.*15_*21delinsCCATTCT ENSP00000364401.3:n.*15_*21delinsCCATTCT
ENST00000409484.5:c.524_530delinsCCATTCT ENSP00000386739.1:p.Thr175=
NM_001127383.1:c.*15_*21delinsCCATTCT NP_001120855.1:n.*15_*21delinsCCATTCT
NM_001256909.1:c.524_530delinsCCATTCT NP_001243838.1:p.Thr175=
NM_024843.3:c.698_704delinsCCATTCT NP_079119.3:p.Thr233=
NM_024843.4:c.698_704delinsCCATTCT MANE Select NP_079119.3:p.Thr233=
NM_001127383.2:c.*15_*21delinsCCATTCT NP_001120855.1:n.*15_*21delinsCCATTCT
NM_001256909.2:c.524_530delinsCCATTCT NP_001243838.1:p.Thr175=
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