Canonical Allele Identifier: CA1216149880

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203594_193203596delinsCTT , CM000663.2:g.193203594_193203596delinsCTT	GRCh38
NC_000001.10:g.193172724_193172726delinsCTT , CM000663.1:g.193172724_193172726delinsCTT	GRCh37
NC_000001.9:g.191439347_191439349delinsCTT	NCBI36
NG_012691.1:g.86637_86639delinsCTT , LRG_507:g.86637_86639delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-201_973-199delinsCTT MANE Select	ENSP00000356405.4:n.973-201_973-199delinsCTT
ENST00000635846.1:c.730-201_730-199delinsCTT	ENSP00000490035.1:n.730-201_730-199delinsCTT
ENST00000643006.1:c.1041-201_1041-199delinsCTT	ENSP00000496633.1:n.1041-201_1041-199delinsCTT
ENST00000648071.1:c.*949-201_*949-199delinsCTT	ENSP00000497513.1:n.*949-201_*949-199delinsCTT
ENST00000649613.1:n.223-201_223-199delinsCTT
ENST00000649895.1:n.1191-201_1191-199delinsCTT
ENST00000650197.1:c.973-201_973-199delinsCTT	ENSP00000496929.1:n.973-201_973-199delinsCTT
ENST00000367435.3:c.973-201_973-199delinsCTT	ENSP00000356405.3:n.973-201_973-199delinsCTT
NM_024529.4:c.973-201_973-199delinsCTT , LRG_507t1:c.973-201_973-199delinsCTT	NP_078805.3:n.973-201_973-199delinsCTT
NM_024529.5:c.973-201_973-199delinsCTT MANE Select	NP_078805.3:n.973-201_973-199delinsCTT