Canonical Allele Identifier: CA9359368

Gene: CEP89

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32923514A>G , CM000681.2:g.32923514A>G	GRCh38
NC_000019.9:g.33414420A>G , CM000681.1:g.33414420A>G	GRCh37
NC_000019.8:g.38106260A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305768.10:c.1193T>C MANE Select	ENSP00000306105.4:p.Val398Ala
ENST00000305768.9:c.1193T>C	ENSP00000306105.4:p.Val398Ala
ENST00000586984.6:c.1164+2676T>C	ENSP00000465141.1:n.1164+2676T>C
ENST00000591698.5:c.1049T>C	ENSP00000467544.1:n.1049T>C
NM_032816.4:c.1193T>C	NP_116205.3:p.Val398Ala
XM_005259344.2:c.1164+2676T>C	XP_005259401.1:n.1164+2676T>C
XM_005259346.2:c.1193T>C	XP_005259403.1:p.Val398Ala
XM_011527425.1:c.452T>C	XP_011525727.1:p.Val151Ala
XR_935866.1:n.1314+2676T>C
XM_005259344.3:c.1164+2676T>C	XP_005259401.1:n.1164+2676T>C
XM_017027398.1:c.1193T>C	XP_016882887.1:p.Val398Ala
XM_024451745.1:c.452T>C	XP_024307513.1:p.Val151Ala
XR_002958372.1:n.1343T>C
XR_935866.2:n.1314+2676T>C
NM_032816.5:c.1193T>C MANE Select	NP_116205.3:p.Val398Ala