Canonical Allele Identifier: CA1216149999

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203889_193203896delinsAAAGATCG , CM000663.2:g.193203889_193203896delinsAAAGATCG	GRCh38
NC_000001.10:g.193173019_193173026delinsAAAGATCG , CM000663.1:g.193173019_193173026delinsAAAGATCG	GRCh37
NC_000001.9:g.191439642_191439649delinsAAAGATCG	NCBI36
NG_012691.1:g.86932_86939delinsAAAGATCG , LRG_507:g.86932_86939delinsAAAGATCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+37_1030+44delinsAAAGATCG MANE Select	ENSP00000356405.4:n.1030+37_1030+44delinsAAAGATCG
ENST00000635846.1:c.787+37_787+44delinsAAAGATCG	ENSP00000490035.1:n.787+37_787+44delinsAAAGATCG
ENST00000643006.1:c.1098+37_1098+44delinsAAAGATCG	ENSP00000496633.1:n.1098+37_1098+44delinsAAAGATCG
ENST00000648071.1:c.*1006+37_*1006+44delinsAAAGATCG	ENSP00000497513.1:n.*1006+37_*1006+44delinsAAAGATCG
ENST00000649613.1:n.280+37_280+44delinsAAAGATCG
ENST00000649895.1:n.1248+37_1248+44delinsAAAGATCG
ENST00000650197.1:c.1030+37_1030+44delinsAAAGATCG	ENSP00000496929.1:n.1030+37_1030+44delinsAAAGATCG
ENST00000367435.3:c.1030+37_1030+44delinsAAAGATCG	ENSP00000356405.3:n.1030+37_1030+44delinsAAAGATCG
NM_024529.4:c.1030+37_1030+44delinsAAAGATCG , LRG_507t1:c.1030+37_1030+44delinsAAAGATCG	NP_078805.3:n.1030+37_1030+44delinsAAAGATCG
NM_024529.5:c.1030+37_1030+44delinsAAAGATCG MANE Select	NP_078805.3:n.1030+37_1030+44delinsAAAGATCG