Canonical Allele Identifier: CA1145432807
Gene: CDC73 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122038C= , CM000663.2:g.193122038C= GRCh38
NC_000001.10:g.193091168C= , CM000663.1:g.193091168C= GRCh37
NC_000001.9:g.191357791C= NCBI36
NG_012691.1:g.5081C= , LRG_507:g.5081C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.-163C= MANE Select ENSP00000356405.4:n.-163C=
ENST00000643006.1:c.-163C= ENSP00000496633.1:n.-163C=
ENST00000649895.1:n.56C=
ENST00000367435.3:c.-163C= ENSP00000356405.3:n.-163C=
NM_024529.4:c.-163C= , LRG_507t1:c.-163C= NP_078805.3:n.-163C=
XM_006711537.2:c.-163C= XP_006711600.1:n.-163C=
XM_006711537.4:c.-163C= XP_006711600.1:n.-163C=
XR_001738350.1:n.1619G=
NM_024529.5:c.-163C= MANE Select NP_078805.3:n.-163C=