Canonical Allele Identifier: CA1547390796

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233438A= , CM000667.2:g.55233438A=	GRCh38
NC_000005.9:g.54529266A= , CM000667.1:g.54529266A=	GRCh37
NC_000005.8:g.54565023A=	NCBI36
NG_034201.1:g.5280T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.86T= MANE Select	ENSP00000282572.4:p.Val29=
ENST00000282572.4:c.86T=	ENSP00000282572.4:p.Val29=
ENST00000501463.2:c.86T=	ENSP00000422485.1:p.Val29=
NM_021147.4:c.86T=	NP_066970.3:p.Val29=
NR_125346.1:n.280T=
NR_125347.1:n.280T=
NM_021147.5:c.86T= MANE Select	NP_066970.3:p.Val29=
NR_125346.2:n.171T=
NR_125347.2:n.171T=