Canonical Allele Identifier: CA1216150029

Gene: CDC73

Linked Data

• dbSNP Id: rs1677136127

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193204000T>G , CM000663.2:g.193204000T>G	GRCh38
NC_000001.10:g.193173130T>G , CM000663.1:g.193173130T>G	GRCh37
NC_000001.9:g.191439753T>G	NCBI36
NG_012691.1:g.87043T>G , LRG_507:g.87043T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+148T>G MANE Select	ENSP00000356405.4:n.1030+148T>G
ENST00000635846.1:c.787+148T>G	ENSP00000490035.1:n.787+148T>G
ENST00000643006.1:c.1098+148T>G	ENSP00000496633.1:n.1098+148T>G
ENST00000648071.1:c.*1006+148T>G	ENSP00000497513.1:n.*1006+148T>G
ENST00000649613.1:n.280+148T>G
ENST00000649895.1:n.1248+148T>G
ENST00000650197.1:c.1030+148T>G	ENSP00000496929.1:n.1030+148T>G
ENST00000367435.3:c.1030+148T>G	ENSP00000356405.3:n.1030+148T>G
NM_024529.4:c.1030+148T>G , LRG_507t1:c.1030+148T>G	NP_078805.3:n.1030+148T>G
NM_024529.5:c.1030+148T>G MANE Select	NP_078805.3:n.1030+148T>G