Canonical Allele Identifier: CA2499214361

Gene: CDC73

Linked Data

• ClinVar Variation Id: 1131679
• ClinVar RCV Id: RCV001465623
• dbSNP Id: rs2103178136

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203861_193203862insC , CM000663.2:g.193203861_193203862insC	GRCh38
NC_000001.10:g.193172991_193172992insC , CM000663.1:g.193172991_193172992insC	GRCh37
NC_000001.9:g.191439614_191439615insC	NCBI36
NG_012691.1:g.86904_86905insC , LRG_507:g.86904_86905insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+9_1030+10insC MANE Select	ENSP00000356405.4:n.1030+9_1030+10insC
ENST00000635846.1:c.787+9_787+10insC	ENSP00000490035.1:n.787+9_787+10insC
ENST00000643006.1:c.1098+9_1098+10insC	ENSP00000496633.1:n.1098+9_1098+10insC
ENST00000648071.1:c.*1006+9_*1006+10insC	ENSP00000497513.1:n.*1006+9_*1006+10insC
ENST00000649613.1:n.280+9_280+10insC
ENST00000649895.1:n.1248+9_1248+10insC
ENST00000650197.1:c.1030+9_1030+10insC	ENSP00000496929.1:n.1030+9_1030+10insC
ENST00000367435.3:c.1030+9_1030+10insC	ENSP00000356405.3:n.1030+9_1030+10insC
NM_024529.4:c.1030+9_1030+10insC , LRG_507t1:c.1030+9_1030+10insC	NP_078805.3:n.1030+9_1030+10insC
NM_024529.5:c.1030+9_1030+10insC MANE Select	NP_078805.3:n.1030+9_1030+10insC