Canonical Allele Identifier: CA1591288153
Gene: CCDC69 HGNC NCBI

Linked Data

dbSNP Id: rs1752851737

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151206231G>A , CM000667.2:g.151206231G>A GRCh38
NC_000005.9:g.150585792G>A , CM000667.1:g.150585792G>A GRCh37
NC_000005.8:g.150565985G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000355417.7:c.49-756C>T MANE Select ENSP00000347586.2:n.49-756C>T
ENST00000355417.6:c.49-756C>T ENSP00000347586.2:n.49-756C>T
ENST00000521308.5:n.172-4543C>T
ENST00000522179.1:n.491-756C>T
NM_015621.2:c.49-756C>T NP_056436.2:n.49-756C>T
NM_015621.3:c.49-756C>T MANE Select NP_056436.2:n.49-756C>T