Canonical Allele Identifier: CA2648610998

Gene: CFAP45

Linked Data

• gnomAD v4: 1-159886437-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886440del , CM000663.2:g.159886440del	GRCh38
NC_000001.10:g.159856230del , CM000663.1:g.159856230del	GRCh37
NC_000001.9:g.158122854del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.767+73del MANE Select	ENSP00000357079.4:n.767+73del
ENST00000368099.8:c.767+73del	ENSP00000357079.4:n.767+73del
ENST00000426543.6:c.512+73del	ENSP00000403044.2:n.512+73del
ENST00000476696.5:c.767+73del	ENSP00000483972.1:n.767+73del
NM_012337.2:c.767+73del	NP_036469.2:n.767+73del
NM_012337.3:c.767+73del MANE Select	NP_036469.2:n.767+73del