Canonical Allele Identifier: CA1216150042

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193204017_193204019delinsCTG , CM000663.2:g.193204017_193204019delinsCTG	GRCh38
NC_000001.10:g.193173147_193173149delinsCTG , CM000663.1:g.193173147_193173149delinsCTG	GRCh37
NC_000001.9:g.191439770_191439772delinsCTG	NCBI36
NG_012691.1:g.87060_87062delinsCTG , LRG_507:g.87060_87062delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+165_1030+167delinsCTG MANE Select	ENSP00000356405.4:n.1030+165_1030+167delinsCTG
ENST00000635846.1:c.787+165_787+167delinsCTG	ENSP00000490035.1:n.787+165_787+167delinsCTG
ENST00000643006.1:c.1098+165_1098+167delinsCTG	ENSP00000496633.1:n.1098+165_1098+167delinsCTG
ENST00000648071.1:c.*1006+165_*1006+167delinsCTG	ENSP00000497513.1:n.*1006+165_*1006+167delinsCTG
ENST00000649613.1:n.280+165_280+167delinsCTG
ENST00000649895.1:n.1248+165_1248+167delinsCTG
ENST00000650197.1:c.1030+165_1030+167delinsCTG	ENSP00000496929.1:n.1030+165_1030+167delinsCTG
ENST00000367435.3:c.1030+165_1030+167delinsCTG	ENSP00000356405.3:n.1030+165_1030+167delinsCTG
NM_024529.4:c.1030+165_1030+167delinsCTG , LRG_507t1:c.1030+165_1030+167delinsCTG	NP_078805.3:n.1030+165_1030+167delinsCTG
NM_024529.5:c.1030+165_1030+167delinsCTG MANE Select	NP_078805.3:n.1030+165_1030+167delinsCTG