Canonical Allele Identifier: CA2648610916

Gene: CFAP45

Linked Data

• gnomAD v4: 1-159886370-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886371dup , CM000663.2:g.159886371dup	GRCh38
NC_000001.10:g.159856161dup , CM000663.1:g.159856161dup	GRCh37
NC_000001.9:g.158122785dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.767+140dup MANE Select	ENSP00000357079.4:n.767+140dup
ENST00000368099.8:c.767+140dup	ENSP00000357079.4:n.767+140dup
ENST00000426543.6:c.512+140dup	ENSP00000403044.2:n.512+140dup
ENST00000476696.5:c.767+140dup	ENSP00000483972.1:n.767+140dup
NM_012337.2:c.767+140dup	NP_036469.2:n.767+140dup
NM_012337.3:c.767+140dup MANE Select	NP_036469.2:n.767+140dup