Canonical Allele Identifier: CA2649598753

Gene: CDC73

Linked Data

• gnomAD v4: 1-193203870-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203870T>C , CM000663.2:g.193203870T>C	GRCh38
NC_000001.10:g.193173000T>C , CM000663.1:g.193173000T>C	GRCh37
NC_000001.9:g.191439623T>C	NCBI36
NG_012691.1:g.86913T>C , LRG_507:g.86913T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+18T>C MANE Select	ENSP00000356405.4:n.1030+18T>C
ENST00000635846.1:c.787+18T>C	ENSP00000490035.1:n.787+18T>C
ENST00000643006.1:c.1098+18T>C	ENSP00000496633.1:n.1098+18T>C
ENST00000648071.1:c.*1006+18T>C	ENSP00000497513.1:n.*1006+18T>C
ENST00000649613.1:n.280+18T>C
ENST00000649895.1:n.1248+18T>C
ENST00000650197.1:c.1030+18T>C	ENSP00000496929.1:n.1030+18T>C
ENST00000367435.3:c.1030+18T>C	ENSP00000356405.3:n.1030+18T>C
NM_024529.4:c.1030+18T>C , LRG_507t1:c.1030+18T>C	NP_078805.3:n.1030+18T>C
NM_024529.5:c.1030+18T>C MANE Select	NP_078805.3:n.1030+18T>C