Canonical Allele Identifier: CA1216149849
Gene: CDC73 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203503C= , CM000663.2:g.193203503C= GRCh38
NC_000001.10:g.193172633C= , CM000663.1:g.193172633C= GRCh37
NC_000001.9:g.191439256C= NCBI36
NG_012691.1:g.86546C= , LRG_507:g.86546C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.973-292C= MANE Select ENSP00000356405.4:n.973-292C=
ENST00000635846.1:c.730-292C= ENSP00000490035.1:n.730-292C=
ENST00000643006.1:c.1041-292C= ENSP00000496633.1:n.1041-292C=
ENST00000648071.1:c.*949-292C= ENSP00000497513.1:n.*949-292C=
ENST00000649613.1:n.223-292C=
ENST00000649895.1:n.1191-292C=
ENST00000650197.1:c.973-292C= ENSP00000496929.1:n.973-292C=
ENST00000367435.3:c.973-292C= ENSP00000356405.3:n.973-292C=
NM_024529.4:c.973-292C= , LRG_507t1:c.973-292C= NP_078805.3:n.973-292C=
NM_024529.5:c.973-292C= MANE Select NP_078805.3:n.973-292C=
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