Canonical Allele Identifier: CA1216113280
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122034A= , CM000663.2:g.193122034A= GRCh38
NC_000001.10:g.193091164A= , CM000663.1:g.193091164A= GRCh37
NC_000001.9:g.191357787A= NCBI36
NG_012691.1:g.5077A= , LRG_507:g.5077A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-167A= MANE Select ENSP00000356405.4:n.-167A=
ENST00000643006.1:c.-167A= ENSP00000496633.1:n.-167A=
ENST00000649895.1:n.52A=
ENST00000367435.3:c.-167A= ENSP00000356405.3:n.-167A=
NM_024529.4:c.-167A= , LRG_507t1:c.-167A= NP_078805.3:n.-167A=
XM_006711537.2:c.-167A= XP_006711600.1:n.-167A=
XM_006711537.4:c.-167A= XP_006711600.1:n.-167A=
XR_001738350.1:n.1623T=
NM_024529.5:c.-167A= MANE Select NP_078805.3:n.-167A=