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