Canonical Allele Identifier: CA300033885
Community Standard Title: NM_145020.5(CFAP53):c.877C>T (p.Gln293Ter)
Gene: CFAP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.50250877G>A , CM000680.2:g.50250877G>A GRCh38
NC_000018.9:g.47777247G>A , CM000680.1:g.47777247G>A GRCh37
NC_000018.8:g.46031245G>A NCBI36
NG_042815.1:g.20646C>T

Transcript Alleles

HGVS Amino-acid Change
NM_145020.5:c.877C>T MANE Select NP_659457.2:p.Gln293Ter
ENST00000398545.5:c.877C>T MANE Select ENSP00000381553.3:p.Gln293Ter
NM_145020.3:c.877C>T NP_659457.2:p.Gln293Ter
NM_145020.4:c.877C>T NP_659457.2:p.Gln293Ter
ENST00000398545.4:c.877C>T ENSP00000381553.3:p.Gln293Ter
XM_024451100.1:c.280C>T XP_024306868.1:p.Gln94Ter