Canonical Allele Identifier: CA917396912

Gene: CEP72

Linked Data

• dbSNP Id: rs1579925924

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.618568del , CM000667.2:g.618568del	GRCh38
NC_000005.9:g.618683del , CM000667.1:g.618683del	GRCh37
NC_000005.8:g.671683del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264935.6:c.83-422del MANE Select	ENSP00000264935.5:n.83-422del
ENST00000264935.5:c.83-422del	ENSP00000264935.5:n.83-422del
NM_018140.3:c.83-422del	NP_060610.2:n.83-422del
XM_005248322.2:c.-68-422del	XP_005248379.1:n.-68-422del
XM_011514063.1:c.83-422del	XP_011512365.1:n.83-422del
XM_011514064.1:c.-68-422del	XP_011512366.1:n.-68-422del
XM_011514065.1:c.-68-422del	XP_011512367.1:n.-68-422del
XM_011514066.1:c.-68-422del	XP_011512368.1:n.-68-422del
XR_925628.1:n.101-422del
XR_925630.1:n.101-422del
XR_925631.1:n.101-422del
XM_005248322.3:c.-68-422del	XP_005248379.1:n.-68-422del
XM_011514064.2:c.-68-422del	XP_011512366.1:n.-68-422del
XM_017009626.1:c.-376-422del	XP_016865115.1:n.-376-422del
XM_017009627.1:c.-376-422del	XP_016865116.1:n.-376-422del
XR_001742146.1:n.95-422del
XR_001742147.2:n.78-422del
XR_001742148.1:n.25-422del
XR_001742149.1:n.208-422del
XR_925630.2:n.101-422del
XR_925631.2:n.101-422del
NM_018140.4:c.83-422del MANE Select	NP_060610.2:n.83-422del
NR_164122.1:n.263-422del