Canonical Allele Identifier: CA660176
Gene: CDA HGNC NCBI

Linked Data

dbSNP Id: rs3215400

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20589099del , CM000663.2:g.20589099del GRCh38
NC_000001.10:g.20915592del , CM000663.1:g.20915592del GRCh37
NC_000001.9:g.20788179del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.-31del MANE Select ENSP00000364212.3:n.-31del
ENST00000375071.3:c.-31del ENSP00000364212.3:n.-31del
ENST00000461985.1:n.14del
NM_001785.2:c.-31del NP_001776.1:n.-31del
NM_001785.3:c.-31del MANE Select NP_001776.1:n.-31del