Canonical Allele Identifier: CA444397260

Gene: CCNO

Linked Data

• MyVariant Identifiers: chr5:g.54529196C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233368C>G , CM000667.2:g.55233368C>G	GRCh38
NC_000005.9:g.54529196C>G , CM000667.1:g.54529196C>G	GRCh37
NC_000005.8:g.54564953C>G	NCBI36
NG_034201.1:g.5350G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.156G>C MANE Select	ENSP00000282572.4:p.Pro52=
ENST00000282572.4:c.156G>C	ENSP00000282572.4:p.Pro52=
ENST00000501463.2:c.156G>C	ENSP00000422485.1:p.Pro52=
NM_021147.4:c.156G>C	NP_066970.3:p.Pro52=
NR_125346.1:n.350G>C
NR_125347.1:n.350G>C
NM_021147.5:c.156G>C MANE Select	NP_066970.3:p.Pro52=
NR_125346.2:n.241G>C
NR_125347.2:n.241G>C