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