Canonical Allele Identifier: CA1216171045
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251524C= , CM000663.2:g.193251524C= GRCh38
NC_000001.10:g.193220654C= , CM000663.1:g.193220654C= GRCh37
NC_000001.9:g.191487277C= NCBI36
NG_012691.1:g.134567C= , LRG_507:g.134567C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.*812C= MANE Select ENSP00000356405.4:n.*812C=
ENST00000635846.1:c.*812C= ENSP00000490035.1:n.*812C=
ENST00000643006.1:c.*1318C= ENSP00000496633.1:n.*1318C=
ENST00000367435.3:c.*812C= ENSP00000356405.3:n.*812C=
NM_024529.4:c.*812C= , LRG_507t1:c.*812C= NP_078805.3:n.*812C=
NM_024529.5:c.*812C= MANE Select NP_078805.3:n.*812C=