Canonical Allele Identifier: CA3266826

Gene: CCNO

Linked Data

• dbSNP Id: rs780643778
• ExAC: 5:54529095 G / A
• gnomAD v2: 5-54529095-G-A
• gnomAD v3: 5-55233267-G-A
• gnomAD v4: 5-55233267-G-A
• MyVariant Identifiers: chr5:g.54529095G>A (hg19) ; chr5:g.55233267G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233267G>A , CM000667.2:g.55233267G>A	GRCh38
NC_000005.9:g.54529095G>A , CM000667.1:g.54529095G>A	GRCh37
NC_000005.8:g.54564852G>A	NCBI36
NG_034201.1:g.5451C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.257C>T MANE Select	ENSP00000282572.4:p.Pro86Leu
ENST00000282572.4:c.257C>T	ENSP00000282572.4:p.Pro86Leu
ENST00000501463.2:c.257C>T	ENSP00000422485.1:p.Pro86Leu
NM_021147.4:c.257C>T	NP_066970.3:p.Pro86Leu
NR_125346.1:n.451C>T
NR_125347.1:n.451C>T
NM_021147.5:c.257C>T MANE Select	NP_066970.3:p.Pro86Leu
NR_125346.2:n.342C>T
NR_125347.2:n.342C>T