Canonical Allele Identifier: CA373856476

Gene: CEP78

Linked Data

• MyVariant Identifiers: chr9:g.80863209C>G (hg19) ; chr9:g.78248293C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78248293C>G , CM000671.2:g.78248293C>G	GRCh38
NC_000009.11:g.80863209C>G , CM000671.1:g.80863209C>G	GRCh37
NC_000009.10:g.80053029C>G	NCBI36
NG_053171.1:g.17232C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376597.9:c.895C>G	ENSP00000365782.4:p.His299Asp
ENST00000376598.3:c.895C>G	ENSP00000365783.3:p.His299Asp
ENST00000642214.1:c.895C>G	ENSP00000493662.1:p.His299Asp
ENST00000642654.1:c.*690C>G	ENSP00000495267.1:n.*690C>G
ENST00000642669.1:c.895C>G	ENSP00000495681.1:p.His299Asp
ENST00000643273.2:c.895C>G MANE Select	ENSP00000496423.2:p.His299Asp
ENST00000643347.1:c.895C>G	ENSP00000494781.1:p.His299Asp
ENST00000643499.1:c.895C>G	ENSP00000495962.1:p.His299Asp
ENST00000643847.1:c.781C>G	ENSP00000494276.1:p.His261Asp
ENST00000644208.1:c.895C>G	ENSP00000493600.1:p.His299Asp
ENST00000645398.1:c.895C>G	ENSP00000493822.1:p.His299Asp
ENST00000645865.1:c.*617C>G	ENSP00000494841.1:n.*617C>G
ENST00000646288.1:c.837C>G	ENSP00000496131.1:n.837C>G
ENST00000647130.1:c.930C>G	ENSP00000496303.1:n.930C>G
ENST00000647199.1:c.895C>G	ENSP00000496384.1:p.His299Asp
ENST00000277082.9:c.895C>G	ENSP00000277082.5:p.His299Asp
ENST00000376597.8:c.895C>G	ENSP00000365782.4:p.His299Asp
ENST00000376598.2:c.895C>G	ENSP00000365783.2:p.His299Asp
ENST00000415759.6:c.895C>G	ENSP00000399286.2:p.His299Asp
ENST00000424347.6:c.895C>G	ENSP00000411284.2:p.His299Asp
ENST00000476652.2:n.463+11690C>G
ENST00000536374.1:n.1221C>G
NM_001098802.1:c.895C>G	NP_001092272.1:p.His299Asp
NM_032171.1:c.895C>G	NP_115547.1:p.His299Asp
XM_005252263.3:c.895C>G	XP_005252320.1:p.His299Asp
XM_005252265.1:c.895C>G	XP_005252322.1:p.His299Asp
XM_005252266.3:c.634C>G	XP_005252323.1:p.His212Asp
NM_001098802.2:c.895C>G	NP_001092272.1:p.His299Asp
NM_001330691.2:c.895C>G	NP_001317620.1:p.His299Asp
NM_001330693.2:c.895C>G	NP_001317622.1:p.His299Asp
NM_001330694.1:c.895C>G	NP_001317623.1:p.His299Asp
NM_001349838.1:c.895C>G	NP_001336767.1:p.His299Asp
NM_001349839.1:c.895C>G	NP_001336768.1:p.His299Asp
NM_001349840.1:c.895C>G	NP_001336769.1:p.His299Asp
NM_032171.2:c.895C>G	NP_115547.1:p.His299Asp
XM_005252266.4:c.634C>G	XP_005252323.1:p.His212Asp
XM_017015196.1:c.634C>G	XP_016870685.1:p.His212Asp
NM_001098802.3:c.895C>G	NP_001092272.1:p.His299Asp
NM_001330691.3:c.895C>G MANE Select	NP_001317620.1:p.His299Asp
NM_001330693.3:c.895C>G	NP_001317622.1:p.His299Asp
NM_001330694.2:c.895C>G	NP_001317623.1:p.His299Asp
NM_001349838.2:c.895C>G	NP_001336767.1:p.His299Asp
NM_001349839.2:c.895C>G	NP_001336768.1:p.His299Asp
NM_001349840.2:c.895C>G	NP_001336769.1:p.His299Asp
NM_032171.3:c.895C>G	NP_115547.1:p.His299Asp