Canonical Allele Identifier: CA2574103635
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203701G>A , CM000663.2:g.193203701G>A GRCh38
NC_000001.10:g.193172831G>A , CM000663.1:g.193172831G>A GRCh37
NC_000001.9:g.191439454G>A NCBI36
NG_012691.1:g.86744G>A , LRG_507:g.86744G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.973-94G>A MANE Select ENSP00000356405.4:n.973-94G>A
ENST00000635846.1:c.730-94G>A ENSP00000490035.1:n.730-94G>A
ENST00000643006.1:c.1041-94G>A ENSP00000496633.1:n.1041-94G>A
ENST00000648071.1:c.*949-94G>A ENSP00000497513.1:n.*949-94G>A
ENST00000649613.1:n.223-94G>A
ENST00000649895.1:n.1191-94G>A
ENST00000650197.1:c.973-94G>A ENSP00000496929.1:n.973-94G>A
ENST00000367435.3:c.973-94G>A ENSP00000356405.3:n.973-94G>A
NM_024529.4:c.973-94G>A , LRG_507t1:c.973-94G>A NP_078805.3:n.973-94G>A
NM_024529.5:c.973-94G>A MANE Select NP_078805.3:n.973-94G>A