Canonical Allele Identifier: CA421350588
Gene: CFAP45 HGNC NCBI

Linked Data

gnomAD v4: 1-159886534-C-T
MyVariant Identifiers: chr1:g.159856324C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886534C>T , CM000663.2:g.159886534C>T GRCh38
NC_000001.10:g.159856324C>T , CM000663.1:g.159856324C>T GRCh37
NC_000001.9:g.158122948C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.744G>A MANE Select ENSP00000357079.4:p.Arg248=
ENST00000368099.8:c.744G>A ENSP00000357079.4:p.Arg248=
ENST00000426543.6:c.489G>A ENSP00000403044.2:p.Arg163=
ENST00000476696.5:c.744G>A ENSP00000483972.1:p.Arg248=
NM_012337.2:c.744G>A NP_036469.2:p.Arg248=
NM_012337.3:c.744G>A MANE Select NP_036469.2:p.Arg248=
Search 100 bp 5'
Search 100 bp 3'