Canonical Allele Identifier: CA359725383
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233375-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233375G>A , CM000667.2:g.55233375G>A GRCh38
NC_000005.9:g.54529203G>A , CM000667.1:g.54529203G>A GRCh37
NC_000005.8:g.54564960G>A NCBI36
NG_034201.1:g.5343C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.149C>T MANE Select ENSP00000282572.4:p.Pro50Leu
ENST00000282572.4:c.149C>T ENSP00000282572.4:p.Pro50Leu
ENST00000501463.2:c.149C>T ENSP00000422485.1:p.Pro50Leu
NM_021147.4:c.149C>T NP_066970.3:p.Pro50Leu
NR_125346.1:n.343C>T
NR_125347.1:n.343C>T
NM_021147.5:c.149C>T MANE Select NP_066970.3:p.Pro50Leu
NR_125346.2:n.234C>T
NR_125347.2:n.234C>T