Canonical Allele Identifier: CA2606574996
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs2103177797

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203539_193203543del , CM000663.2:g.193203539_193203543del GRCh38
NC_000001.10:g.193172669_193172673del , CM000663.1:g.193172669_193172673del GRCh37
NC_000001.9:g.191439292_191439296del NCBI36
NG_012691.1:g.86582_86586del , LRG_507:g.86582_86586del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.973-256_973-252del MANE Select ENSP00000356405.4:n.973-256_973-252del
ENST00000635846.1:c.730-256_730-252del ENSP00000490035.1:n.730-256_730-252del
ENST00000643006.1:c.1041-256_1041-252del ENSP00000496633.1:n.1041-256_1041-252del
ENST00000648071.1:c.*949-256_*949-252del ENSP00000497513.1:n.*949-256_*949-252del
ENST00000649613.1:n.223-256_223-252del
ENST00000649895.1:n.1191-256_1191-252del
ENST00000650197.1:c.973-256_973-252del ENSP00000496929.1:n.973-256_973-252del
ENST00000367435.3:c.973-256_973-252del ENSP00000356405.3:n.973-256_973-252del
NM_024529.4:c.973-256_973-252del , LRG_507t1:c.973-256_973-252del NP_078805.3:n.973-256_973-252del
NM_024529.5:c.973-256_973-252del MANE Select NP_078805.3:n.973-256_973-252del