Canonical Allele Identifier: CA1157639768
Gene: CDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618486C= , CM000663.2:g.20618486C= GRCh38
NC_000001.10:g.20944979C= , CM000663.1:g.20944979C= GRCh37
NC_000001.9:g.20817566C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.359C= MANE Select ENSP00000364212.3:p.Pro120=
ENST00000375071.3:c.359C= ENSP00000364212.3:p.Pro120=
ENST00000461985.1:n.345C=
NM_001785.2:c.359C= NP_001776.1:p.Pro120=
NM_001785.3:c.359C= MANE Select NP_001776.1:p.Pro120=