Canonical Allele Identifier: CA1216171174
Gene: CDC73 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193251834A= , CM000663.2:g.193251834A= GRCh38
NC_000001.10:g.193220964A= , CM000663.1:g.193220964A= GRCh37
NC_000001.9:g.191487587A= NCBI36
NG_012691.1:g.134877A= , LRG_507:g.134877A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367435.5:c.*1122A= MANE Select ENSP00000356405.4:n.*1122A=
ENST00000635846.1:c.*1122A= ENSP00000490035.1:n.*1122A=
ENST00000643006.1:c.*1628A= ENSP00000496633.1:n.*1628A=
ENST00000367435.3:c.*1122A= ENSP00000356405.3:n.*1122A=
NM_024529.4:c.*1122A= , LRG_507t1:c.*1122A= NP_078805.3:n.*1122A=
NM_024529.5:c.*1122A= MANE Select NP_078805.3:n.*1122A=
Search 100 bp 5'
Search 100 bp 3'