Canonical Allele Identifier: CA2649624666

Gene: CDC73

Linked Data

• gnomAD v4: 1-193122133-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122133A>C , CM000663.2:g.193122133A>C	GRCh38
NC_000001.10:g.193091263A>C , CM000663.1:g.193091263A>C	GRCh37
NC_000001.9:g.191357886A>C	NCBI36
NG_012691.1:g.5176A>C , LRG_507:g.5176A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-68A>C MANE Select	ENSP00000356405.4:n.-68A>C
ENST00000643006.1:c.-68A>C	ENSP00000496633.1:n.-68A>C
ENST00000643784.1:c.-68A>C	ENSP00000494944.1:n.-68A>C
ENST00000649895.1:n.151A>C
ENST00000650197.1:c.-68A>C	ENSP00000496929.1:n.-68A>C
ENST00000367435.3:c.-68A>C	ENSP00000356405.3:n.-68A>C
NM_024529.4:c.-68A>C , LRG_507t1:c.-68A>C	NP_078805.3:n.-68A>C
XM_006711537.2:c.-68A>C	XP_006711600.1:n.-68A>C
XM_006711537.4:c.-68A>C	XP_006711600.1:n.-68A>C
XR_001738350.1:n.1524T>G
NM_024529.5:c.-68A>C MANE Select	NP_078805.3:n.-68A>C