Canonical Allele Identifier: CA34370739

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193138178G>C , CM000663.2:g.193138178G>C	GRCh38
NC_000001.10:g.193107308G>C , CM000663.1:g.193107308G>C	GRCh37
NC_000001.9:g.191373931G>C	NCBI36
NG_012691.1:g.21221G>C , LRG_507:g.21221G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.512+5G>C MANE Select	NP_078805.3:n.512+5G>C
ENST00000367435.5:c.512+5G>C MANE Select	ENSP00000356405.4:n.512+5G>C
NM_024529.4:c.512+5G>C , LRG_507t1:c.512+5G>C	NP_078805.3:n.512+5G>C
ENST00000367435.3:c.512+5G>C	ENSP00000356405.3:n.512+5G>C
ENST00000635846.1:c.512+5G>C	ENSP00000490035.1:n.512+5G>C
ENST00000643006.1:c.512+5G>C	ENSP00000496633.1:n.512+5G>C
ENST00000643784.1:c.512+5G>C	ENSP00000494944.1:n.512+5G>C
ENST00000647662.1:n.413+5G>C
ENST00000648071.1:c.*488+5G>C	ENSP00000497513.1:n.*488+5G>C
ENST00000649606.1:n.525+5G>C
ENST00000649706.1:n.453+5G>C
ENST00000649895.1:n.730+5G>C
ENST00000650197.1:c.512+5G>C	ENSP00000496929.1:n.512+5G>C
XM_006711537.2:c.512+5G>C	XP_006711600.1:n.512+5G>C
XM_006711537.4:c.512+5G>C	XP_006711600.1:n.512+5G>C