Canonical Allele Identifier: CA374000441

Gene: CEP78

Linked Data

• MyVariant Identifiers: chr9:g.80858408T>A (hg19) ; chr9:g.78243492T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78243492T>A , CM000671.2:g.78243492T>A	GRCh38
NC_000009.11:g.80858408T>A , CM000671.1:g.80858408T>A	GRCh37
NC_000009.10:g.80048228T>A	NCBI36
NG_053171.1:g.12431T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376597.9:c.634T>A	ENSP00000365782.4:p.Trp212Arg
ENST00000376598.3:c.634T>A	ENSP00000365783.3:p.Trp212Arg
ENST00000642214.1:c.634T>A	ENSP00000493662.1:p.Trp212Arg
ENST00000642654.1:c.*429T>A	ENSP00000495267.1:n.*429T>A
ENST00000642669.1:c.634T>A	ENSP00000495681.1:p.Trp212Arg
ENST00000643273.2:c.634T>A MANE Select	ENSP00000496423.2:p.Trp212Arg
ENST00000643347.1:c.634T>A	ENSP00000494781.1:p.Trp212Arg
ENST00000643499.1:c.634T>A	ENSP00000495962.1:p.Trp212Arg
ENST00000643847.1:c.634T>A	ENSP00000494276.1:p.Trp212Arg
ENST00000644208.1:c.634T>A	ENSP00000493600.1:p.Trp212Arg
ENST00000645398.1:c.634T>A	ENSP00000493822.1:p.Trp212Arg
ENST00000645865.1:c.*356T>A	ENSP00000494841.1:n.*356T>A
ENST00000646288.1:c.690T>A	ENSP00000496131.1:n.690T>A
ENST00000647130.1:c.669T>A	ENSP00000496303.1:n.669T>A
ENST00000647199.1:c.634T>A	ENSP00000496384.1:p.Trp212Arg
ENST00000277082.9:c.634T>A	ENSP00000277082.5:p.Trp212Arg
ENST00000376597.8:c.634T>A	ENSP00000365782.4:p.Trp212Arg
ENST00000376598.2:c.634T>A	ENSP00000365783.2:p.Trp212Arg
ENST00000415759.6:c.634T>A	ENSP00000399286.2:p.Trp212Arg
ENST00000424347.6:c.634T>A	ENSP00000411284.2:p.Trp212Arg
ENST00000476652.2:n.463+6889T>A
ENST00000536374.1:n.960T>A
NM_001098802.1:c.634T>A	NP_001092272.1:p.Trp212Arg
NM_032171.1:c.634T>A	NP_115547.1:p.Trp212Arg
XM_005252263.3:c.634T>A	XP_005252320.1:p.Trp212Arg
XM_005252265.1:c.634T>A	XP_005252322.1:p.Trp212Arg
XM_005252266.3:c.373T>A	XP_005252323.1:p.Trp125Arg
NM_001098802.2:c.634T>A	NP_001092272.1:p.Trp212Arg
NM_001330691.2:c.634T>A	NP_001317620.1:p.Trp212Arg
NM_001330693.2:c.634T>A	NP_001317622.1:p.Trp212Arg
NM_001330694.1:c.634T>A	NP_001317623.1:p.Trp212Arg
NM_001349838.1:c.634T>A	NP_001336767.1:p.Trp212Arg
NM_001349839.1:c.634T>A	NP_001336768.1:p.Trp212Arg
NM_001349840.1:c.634T>A	NP_001336769.1:p.Trp212Arg
NM_032171.2:c.634T>A	NP_115547.1:p.Trp212Arg
XM_005252266.4:c.373T>A	XP_005252323.1:p.Trp125Arg
XM_017015196.1:c.373T>A	XP_016870685.1:p.Trp125Arg
NM_001098802.3:c.634T>A	NP_001092272.1:p.Trp212Arg
NM_001330691.3:c.634T>A MANE Select	NP_001317620.1:p.Trp212Arg
NM_001330693.3:c.634T>A	NP_001317622.1:p.Trp212Arg
NM_001330694.2:c.634T>A	NP_001317623.1:p.Trp212Arg
NM_001349838.2:c.634T>A	NP_001336767.1:p.Trp212Arg
NM_001349839.2:c.634T>A	NP_001336768.1:p.Trp212Arg
NM_001349840.2:c.634T>A	NP_001336769.1:p.Trp212Arg
NM_032171.3:c.634T>A	NP_115547.1:p.Trp212Arg