Canonical Allele Identifier: CA2927459

Gene: CEP135

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55952252A>G , CM000666.2:g.55952252A>G	GRCh38
NC_000004.11:g.56818418A>G , CM000666.1:g.56818418A>G	GRCh37
NC_000004.10:g.56513175A>G	NCBI36
NG_032806.1:g.8445A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025009.5:c.113+9A>G MANE Select	NP_079285.2:n.113+9A>G
ENST00000257287.5:c.113+9A>G MANE Select	ENSP00000257287.3:n.113+9A>G
NM_025009.4:c.113+9A>G	NP_079285.2:n.113+9A>G
ENST00000257287.4:c.113+9A>G	ENSP00000257287.3:n.113+9A>G
ENST00000422247.6:c.113+9A>G	ENSP00000412799.2:n.113+9A>G
ENST00000506809.1:n.282A>G
ENST00000706800.1:n.286+9A>G
XM_005265788.4:c.-955+9A>G	XP_005265845.1:n.-955+9A>G
XM_006714055.2:c.113+9A>G	XP_006714118.1:n.113+9A>G
XM_006714055.3:c.113+9A>G	XP_006714118.1:n.113+9A>G
XR_941064.1:n.650+41T>C