Canonical Allele Identifier: CA96958301

Gene: CEP135

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55965423T>C , CM000666.2:g.55965423T>C	GRCh38
NC_000004.11:g.56831589T>C , CM000666.1:g.56831589T>C	GRCh37
NC_000004.10:g.56526346T>C	NCBI36
NG_032806.1:g.21616T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257287.5:c.829-221T>C MANE Select	ENSP00000257287.3:n.829-221T>C
ENST00000257287.4:c.829-221T>C	ENSP00000257287.3:n.829-221T>C
ENST00000506202.1:n.558T>C
ENST00000515081.1:n.463-221T>C
NM_025009.4:c.829-221T>C	NP_079285.2:n.829-221T>C
XM_006714055.2:c.829-221T>C	XP_006714118.1:n.829-221T>C
XR_941063.1:n.472-420A>G
XR_941064.1:n.471+5350A>G
XM_005265788.4:c.-239-221T>C	XP_005265845.1:n.-239-221T>C
XM_006714055.3:c.829-221T>C	XP_006714118.1:n.829-221T>C
NM_025009.5:c.829-221T>C MANE Select	NP_079285.2:n.829-221T>C