Canonical Allele Identifier: CA2765015633
Gene: CEP72 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.618372A>G , CM000667.2:g.618372A>G GRCh38
NC_000005.9:g.618487A>G , CM000667.1:g.618487A>G GRCh37
NC_000005.8:g.671487A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264935.6:c.83-618A>G MANE Select ENSP00000264935.5:n.83-618A>G
ENST00000264935.5:c.83-618A>G ENSP00000264935.5:n.83-618A>G
NM_018140.3:c.83-618A>G NP_060610.2:n.83-618A>G
XM_005248322.2:c.-68-618A>G XP_005248379.1:n.-68-618A>G
XM_011514063.1:c.83-618A>G XP_011512365.1:n.83-618A>G
XM_011514064.1:c.-68-618A>G XP_011512366.1:n.-68-618A>G
XM_011514065.1:c.-69+523A>G XP_011512367.1:n.-69+523A>G
XM_011514066.1:c.-68-618A>G XP_011512368.1:n.-68-618A>G
XR_925628.1:n.101-618A>G
XR_925630.1:n.101-618A>G
XR_925631.1:n.101-618A>G
XM_005248322.3:c.-68-618A>G XP_005248379.1:n.-68-618A>G
XM_011514064.2:c.-68-618A>G XP_011512366.1:n.-68-618A>G
XM_017009626.1:c.-376-618A>G XP_016865115.1:n.-376-618A>G
XM_017009627.1:c.-376-618A>G XP_016865116.1:n.-376-618A>G
XR_001742146.1:n.95-618A>G
XR_001742147.2:n.78-618A>G
XR_001742148.1:n.24+523A>G
XR_001742149.1:n.208-618A>G
XR_925630.2:n.101-618A>G
XR_925631.2:n.101-618A>G
NM_018140.4:c.83-618A>G MANE Select NP_060610.2:n.83-618A>G
NR_164122.1:n.263-618A>G