Canonical Allele Identifier: CA2573970801
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122141A>G , CM000663.2:g.193122141A>G GRCh38
NC_000001.10:g.193091271A>G , CM000663.1:g.193091271A>G GRCh37
NC_000001.9:g.191357894A>G NCBI36
NG_012691.1:g.5184A>G , LRG_507:g.5184A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-60A>G MANE Select ENSP00000356405.4:n.-60A>G
ENST00000643006.1:c.-60A>G ENSP00000496633.1:n.-60A>G
ENST00000643784.1:c.-60A>G ENSP00000494944.1:n.-60A>G
ENST00000649895.1:n.159A>G
ENST00000650197.1:c.-60A>G ENSP00000496929.1:n.-60A>G
ENST00000367435.3:c.-60A>G ENSP00000356405.3:n.-60A>G
NM_024529.4:c.-60A>G , LRG_507t1:c.-60A>G NP_078805.3:n.-60A>G
XM_006711537.2:c.-60A>G XP_006711600.1:n.-60A>G
XM_006711537.4:c.-60A>G XP_006711600.1:n.-60A>G
XR_001738350.1:n.1516T>C
NM_024529.5:c.-60A>G MANE Select NP_078805.3:n.-60A>G