Canonical Allele Identifier: CA1157639569
Gene: CDA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618387A= , CM000663.2:g.20618387A= GRCh38
NC_000001.10:g.20944880A= , CM000663.1:g.20944880A= GRCh37
NC_000001.9:g.20817467A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.325-65A= MANE Select ENSP00000364212.3:n.325-65A=
ENST00000375071.3:c.325-65A= ENSP00000364212.3:n.325-65A=
ENST00000461985.1:n.311-65A=
NM_001785.2:c.325-65A= NP_001776.1:n.325-65A=
NM_001785.3:c.325-65A= MANE Select NP_001776.1:n.325-65A=
Search 100 bp 5'
Search 100 bp 3'