Canonical Allele Identifier: CA9441312
Gene: CCNP HGNC NCBI

Linked Data

ClinVar Variation Id: 3139990
ClinVar RCV Id: RCV004430814
dbSNP Id: rs754924025

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40226490C>T , CM000681.2:g.40226490C>T GRCh38
NC_000019.9:g.40732397C>T , CM000681.1:g.40732397C>T GRCh37
NC_000019.8:g.45424237C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430325.7:c.152G>A MANE Select ENSP00000396755.2:p.Gly51Asp
ENST00000599263.6:c.152G>A ENSP00000470643.2:p.Gly51Asp
ENST00000221818.5:c.152G>A ENSP00000221818.1:p.Gly51Asp
ENST00000430325.6:c.152G>A ENSP00000396755.2:p.Gly51Asp
NM_024877.3:c.152G>A NP_079153.2:p.Gly51Asp
XM_006723395.2:c.356G>A XP_006723458.2:p.Gly119Asp
XR_430212.2:n.606G>A
XR_935860.1:n.606G>A
XR_935861.1:n.606G>A
XM_006723395.3:c.356G>A XP_006723458.2:p.Gly119Asp
XR_001753763.1:n.622G>A
XR_935861.2:n.622G>A
NM_024877.4:c.152G>A MANE Select NP_079153.2:p.Gly51Asp