Canonical Allele Identifier: CA2643867531

Gene: CDA

Linked Data

• gnomAD v4: 1-20618381-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.20618381A>T , CM000663.2:g.20618381A>T	GRCh38
NC_000001.10:g.20944874A>T , CM000663.1:g.20944874A>T	GRCh37
NC_000001.9:g.20817461A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375071.4:c.325-71A>T MANE Select	ENSP00000364212.3:n.325-71A>T
ENST00000375071.3:c.325-71A>T	ENSP00000364212.3:n.325-71A>T
ENST00000461985.1:n.311-71A>T
NM_001785.2:c.325-71A>T	NP_001776.1:n.325-71A>T
NM_001785.3:c.325-71A>T MANE Select	NP_001776.1:n.325-71A>T