Canonical Allele Identifier: CA2768911990
Gene: CCDC69 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151206214G>T , CM000667.2:g.151206214G>T GRCh38
NC_000005.9:g.150585775G>T , CM000667.1:g.150585775G>T GRCh37
NC_000005.8:g.150565968G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000355417.7:c.49-739C>A MANE Select ENSP00000347586.2:n.49-739C>A
ENST00000355417.6:c.49-739C>A ENSP00000347586.2:n.49-739C>A
ENST00000521308.5:n.172-4526C>A
ENST00000522179.1:n.491-739C>A
NM_015621.2:c.49-739C>A NP_056436.2:n.49-739C>A
NM_015621.3:c.49-739C>A MANE Select NP_056436.2:n.49-739C>A