Canonical Allele Identifier: CA2649598807

Gene: CDC73

Linked Data

• gnomAD v4: 1-193203986-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203986A>C , CM000663.2:g.193203986A>C	GRCh38
NC_000001.10:g.193173116A>C , CM000663.1:g.193173116A>C	GRCh37
NC_000001.9:g.191439739A>C	NCBI36
NG_012691.1:g.87029A>C , LRG_507:g.87029A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+134A>C MANE Select	ENSP00000356405.4:n.1030+134A>C
ENST00000635846.1:c.787+134A>C	ENSP00000490035.1:n.787+134A>C
ENST00000643006.1:c.1098+134A>C	ENSP00000496633.1:n.1098+134A>C
ENST00000648071.1:c.*1006+134A>C	ENSP00000497513.1:n.*1006+134A>C
ENST00000649613.1:n.280+134A>C
ENST00000649895.1:n.1248+134A>C
ENST00000650197.1:c.1030+134A>C	ENSP00000496929.1:n.1030+134A>C
ENST00000367435.3:c.1030+134A>C	ENSP00000356405.3:n.1030+134A>C
NM_024529.4:c.1030+134A>C , LRG_507t1:c.1030+134A>C	NP_078805.3:n.1030+134A>C
NM_024529.5:c.1030+134A>C MANE Select	NP_078805.3:n.1030+134A>C