Canonical Allele Identifier: CA343219876
Gene: CFAP45 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.159856388C>G (hg19) chr1:g.159886598C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886598C>G , CM000663.2:g.159886598C>G GRCh38
NC_000001.10:g.159856388C>G , CM000663.1:g.159856388C>G GRCh37
NC_000001.9:g.158123012C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.680G>C MANE Select ENSP00000357079.4:p.Arg227Pro
ENST00000368099.8:c.680G>C ENSP00000357079.4:p.Arg227Pro
ENST00000426543.6:c.425G>C ENSP00000403044.2:p.Arg142Pro
ENST00000476696.5:c.680G>C ENSP00000483972.1:p.Arg227Pro
NM_012337.2:c.680G>C NP_036469.2:p.Arg227Pro
NM_012337.3:c.680G>C MANE Select NP_036469.2:p.Arg227Pro
Search 100 bp 5'
Search 100 bp 3'