Canonical Allele Identifier: CA1522187642

Gene: CEP72

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.618508G= , CM000667.2:g.618508G=	GRCh38
NC_000005.9:g.618623G= , CM000667.1:g.618623G=	GRCh37
NC_000005.8:g.671623G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264935.6:c.83-482G= MANE Select	ENSP00000264935.5:n.83-482G=
ENST00000264935.5:c.83-482G=	ENSP00000264935.5:n.83-482G=
NM_018140.3:c.83-482G=	NP_060610.2:n.83-482G=
XM_005248322.2:c.-68-482G=	XP_005248379.1:n.-68-482G=
XM_011514063.1:c.83-482G=	XP_011512365.1:n.83-482G=
XM_011514064.1:c.-68-482G=	XP_011512366.1:n.-68-482G=
XM_011514065.1:c.-68-482G=	XP_011512367.1:n.-68-482G=
XM_011514066.1:c.-68-482G=	XP_011512368.1:n.-68-482G=
XR_925628.1:n.101-482G=
XR_925630.1:n.101-482G=
XR_925631.1:n.101-482G=
XM_005248322.3:c.-68-482G=	XP_005248379.1:n.-68-482G=
XM_011514064.2:c.-68-482G=	XP_011512366.1:n.-68-482G=
XM_017009626.1:c.-376-482G=	XP_016865115.1:n.-376-482G=
XM_017009627.1:c.-376-482G=	XP_016865116.1:n.-376-482G=
XR_001742146.1:n.95-482G=
XR_001742147.2:n.78-482G=
XR_001742148.1:n.25-482G=
XR_001742149.1:n.208-482G=
XR_925630.2:n.101-482G=
XR_925631.2:n.101-482G=
NM_018140.4:c.83-482G= MANE Select	NP_060610.2:n.83-482G=
NR_164122.1:n.263-482G=