Canonical Allele Identifier: CA1591288147
Gene: CCDC69 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151206210G= , CM000667.2:g.151206210G= GRCh38
NC_000005.9:g.150585771G= , CM000667.1:g.150585771G= GRCh37
NC_000005.8:g.150565964G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000355417.7:c.49-735C= MANE Select ENSP00000347586.2:n.49-735C=
ENST00000355417.6:c.49-735C= ENSP00000347586.2:n.49-735C=
ENST00000521308.5:n.172-4522C=
ENST00000522179.1:n.491-735C=
NM_015621.2:c.49-735C= NP_056436.2:n.49-735C=
NM_015621.3:c.49-735C= MANE Select NP_056436.2:n.49-735C=
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