Canonical Allele Identifier: CA1202094269

Gene: CFAP45

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159886427_159886434delinsTCTCTTCC , CM000663.2:g.159886427_159886434delinsTCTCTTCC	GRCh38
NC_000001.10:g.159856217_159856224delinsTCTCTTCC , CM000663.1:g.159856217_159856224delinsTCTCTTCC	GRCh37
NC_000001.9:g.158122841_158122848delinsTCTCTTCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368099.9:c.767+77_767+84delinsGGAAGAGA MANE Select	ENSP00000357079.4:n.767+77_767+84delinsGGAAGAGA
ENST00000368099.8:c.767+77_767+84delinsGGAAGAGA	ENSP00000357079.4:n.767+77_767+84delinsGGAAGAGA
ENST00000426543.6:c.512+77_512+84delinsGGAAGAGA	ENSP00000403044.2:n.512+77_512+84delinsGGAAGAGA
ENST00000476696.5:c.767+77_767+84delinsGGAAGAGA	ENSP00000483972.1:n.767+77_767+84delinsGGAAGAGA
NM_012337.2:c.767+77_767+84delinsGGAAGAGA	NP_036469.2:n.767+77_767+84delinsGGAAGAGA
NM_012337.3:c.767+77_767+84delinsGGAAGAGA MANE Select	NP_036469.2:n.767+77_767+84delinsGGAAGAGA