Canonical Allele Identifier: CA1216170435

Gene: CDC73

Linked Data

• dbSNP Id: rs1678019860
• gnomAD v4: 1-193249948-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193249948G>C , CM000663.2:g.193249948G>C	GRCh38
NC_000001.10:g.193219078G>C , CM000663.1:g.193219078G>C	GRCh37
NC_000001.9:g.191485701G>C	NCBI36
NG_012691.1:g.132991G>C , LRG_507:g.132991G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1559+77G>C MANE Select	ENSP00000356405.4:n.1559+77G>C
ENST00000635846.1:c.1316+77G>C	ENSP00000490035.1:n.1316+77G>C
ENST00000643006.1:c.*469+77G>C	ENSP00000496633.1:n.*469+77G>C
ENST00000648071.1:c.*1535+77G>C	ENSP00000497513.1:n.*1535+77G>C
ENST00000649613.1:n.809+77G>C
ENST00000650197.1:c.*257+77G>C	ENSP00000496929.1:n.*257+77G>C
ENST00000367435.3:c.1559+77G>C	ENSP00000356405.3:n.1559+77G>C
ENST00000477868.1:n.271+77G>C
NM_024529.4:c.1559+77G>C , LRG_507t1:c.1559+77G>C	NP_078805.3:n.1559+77G>C
NM_024529.5:c.1559+77G>C MANE Select	NP_078805.3:n.1559+77G>C