Canonical Allele Identifier: CA343973023

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193125110A>C , CM000663.2:g.193125110A>C	GRCh38
NC_000001.10:g.193094240A>C , CM000663.1:g.193094240A>C	GRCh37
NC_000001.9:g.191360863A>C	NCBI36
NG_012691.1:g.8153A>C , LRG_507:g.8153A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.132-2A>C MANE Select	NP_078805.3:n.132-2A>C
ENST00000367435.5:c.132-2A>C MANE Select	ENSP00000356405.4:n.132-2A>C
NM_024529.4:c.132-2A>C , LRG_507t1:c.132-2A>C	NP_078805.3:n.132-2A>C
ENST00000367435.3:c.132-2A>C	ENSP00000356405.3:n.132-2A>C
ENST00000482484.1:n.93-2A>C
ENST00000635846.1:c.132-2A>C	ENSP00000490035.1:n.132-2A>C
ENST00000643006.1:c.132-2A>C	ENSP00000496633.1:n.132-2A>C
ENST00000643784.1:c.132-2A>C	ENSP00000494944.1:n.132-2A>C
ENST00000647662.1:n.33-2A>C
ENST00000648071.1:c.132-2A>C	ENSP00000497513.1:n.132-2A>C
ENST00000649606.1:n.145-2A>C
ENST00000649706.1:n.73-2A>C
ENST00000649895.1:n.350-2A>C
ENST00000650197.1:c.132-2A>C	ENSP00000496929.1:n.132-2A>C
XM_006711537.2:c.132-2A>C	XP_006711600.1:n.132-2A>C
XM_006711537.4:c.132-2A>C	XP_006711600.1:n.132-2A>C
XR_241165.2:n.304-803T>G