Canonical Allele Identifier: CA319679
Community Standard Title: NM_145020.5(CFAP53):c.121C>T (p.Arg41Ter)
Gene: CFAP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.50262168G>A , CM000680.2:g.50262168G>A GRCh38
NC_000018.9:g.47788538G>A , CM000680.1:g.47788538G>A GRCh37
NC_000018.8:g.46042536G>A NCBI36
NG_042815.1:g.9355C>T

Transcript Alleles

HGVS Amino-acid Change
NM_145020.5:c.121C>T MANE Select NP_659457.2:p.Arg41Ter
ENST00000398545.5:c.121C>T MANE Select ENSP00000381553.3:p.Arg41Ter
NM_145020.3:c.121C>T NP_659457.2:p.Arg41Ter
NM_145020.4:c.121C>T NP_659457.2:p.Arg41Ter
ENST00000398545.4:c.121C>T ENSP00000381553.3:p.Arg41Ter