Canonical Allele Identifier: CA1157639758
Gene: CDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618480C= , CM000663.2:g.20618480C= GRCh38
NC_000001.10:g.20944973C= , CM000663.1:g.20944973C= GRCh37
NC_000001.9:g.20817560C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.353C= MANE Select ENSP00000364212.3:p.Thr118=
ENST00000375071.3:c.353C= ENSP00000364212.3:p.Thr118=
ENST00000461985.1:n.339C=
NM_001785.2:c.353C= NP_001776.1:p.Thr118=
NM_001785.3:c.353C= MANE Select NP_001776.1:p.Thr118=