Canonical Allele Identifier: CA1157639581
Gene: CDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618392G= , CM000663.2:g.20618392G= GRCh38
NC_000001.10:g.20944885G= , CM000663.1:g.20944885G= GRCh37
NC_000001.9:g.20817472G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.325-60G= MANE Select ENSP00000364212.3:n.325-60G=
ENST00000375071.3:c.325-60G= ENSP00000364212.3:n.325-60G=
ENST00000461985.1:n.311-60G=
NM_001785.2:c.325-60G= NP_001776.1:n.325-60G=
NM_001785.3:c.325-60G= MANE Select NP_001776.1:n.325-60G=