Canonical Allele Identifier: CA1591288187
Gene: CCDC69 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151206316A= , CM000667.2:g.151206316A= GRCh38
NC_000005.9:g.150585877A= , CM000667.1:g.150585877A= GRCh37
NC_000005.8:g.150566070A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000355417.7:c.49-841T= MANE Select ENSP00000347586.2:n.49-841T=
ENST00000355417.6:c.49-841T= ENSP00000347586.2:n.49-841T=
ENST00000521308.5:n.172-4628T=
ENST00000522179.1:n.491-841T=
NM_015621.2:c.49-841T= NP_056436.2:n.49-841T=
NM_015621.3:c.49-841T= MANE Select NP_056436.2:n.49-841T=