Canonical Allele Identifier: CA1216150011

Gene: CDC73

Linked Data

• dbSNP Id: rs1677135090
• gnomAD v4: 1-193203922-TATA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203925_193203927del , CM000663.2:g.193203925_193203927del	GRCh38
NC_000001.10:g.193173055_193173057del , CM000663.1:g.193173055_193173057del	GRCh37
NC_000001.9:g.191439678_191439680del	NCBI36
NG_012691.1:g.86968_86970del , LRG_507:g.86968_86970del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+73_1030+75del MANE Select	ENSP00000356405.4:n.1030+73_1030+75del
ENST00000635846.1:c.787+73_787+75del	ENSP00000490035.1:n.787+73_787+75del
ENST00000643006.1:c.1098+73_1098+75del	ENSP00000496633.1:n.1098+73_1098+75del
ENST00000648071.1:c.*1006+73_*1006+75del	ENSP00000497513.1:n.*1006+73_*1006+75del
ENST00000649613.1:n.280+73_280+75del
ENST00000649895.1:n.1248+73_1248+75del
ENST00000650197.1:c.1030+73_1030+75del	ENSP00000496929.1:n.1030+73_1030+75del
ENST00000367435.3:c.1030+73_1030+75del	ENSP00000356405.3:n.1030+73_1030+75del
NM_024529.4:c.1030+73_1030+75del , LRG_507t1:c.1030+73_1030+75del	NP_078805.3:n.1030+73_1030+75del
NM_024529.5:c.1030+73_1030+75del MANE Select	NP_078805.3:n.1030+73_1030+75del