Canonical Allele Identifier: CA359721329
Gene: CCNO HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.54527522A>C (hg19) chr5:g.55231694A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55231694A>C , CM000667.2:g.55231694A>C GRCh38
NC_000005.9:g.54527522A>C , CM000667.1:g.54527522A>C GRCh37
NC_000005.8:g.54563279A>C NCBI36
NG_034201.1:g.7024T>G
NG_051620.1:g.622T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.734T>G MANE Select ENSP00000282572.4:p.Val245Gly
ENST00000282572.4:c.734T>G ENSP00000282572.4:p.Val245Gly
ENST00000501463.2:c.*714T>G ENSP00000422485.1:n.*714T>G
NM_021147.4:c.734T>G NP_066970.3:p.Val245Gly
NR_125346.1:n.1304T>G
NR_125347.1:n.933T>G
NR_125348.1:n.798T>G
NM_021147.5:c.734T>G MANE Select NP_066970.3:p.Val245Gly
NR_125346.2:n.1195T>G
NR_125347.2:n.824T>G
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