Canonical Allele Identifier: CA1216149889
Gene: CDC73 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203608A= , CM000663.2:g.193203608A= GRCh38
NC_000001.10:g.193172738A= , CM000663.1:g.193172738A= GRCh37
NC_000001.9:g.191439361A= NCBI36
NG_012691.1:g.86651A= , LRG_507:g.86651A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.973-187A= MANE Select ENSP00000356405.4:n.973-187A=
ENST00000635846.1:c.730-187A= ENSP00000490035.1:n.730-187A=
ENST00000643006.1:c.1041-187A= ENSP00000496633.1:n.1041-187A=
ENST00000648071.1:c.*949-187A= ENSP00000497513.1:n.*949-187A=
ENST00000649613.1:n.223-187A=
ENST00000649895.1:n.1191-187A=
ENST00000650197.1:c.973-187A= ENSP00000496929.1:n.973-187A=
ENST00000367435.3:c.973-187A= ENSP00000356405.3:n.973-187A=
NM_024529.4:c.973-187A= , LRG_507t1:c.973-187A= NP_078805.3:n.973-187A=
NM_024529.5:c.973-187A= MANE Select NP_078805.3:n.973-187A=
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