Canonical Allele Identifier: CA1216149926

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203676_193203680delinsCAACT , CM000663.2:g.193203676_193203680delinsCAACT	GRCh38
NC_000001.10:g.193172806_193172810delinsCAACT , CM000663.1:g.193172806_193172810delinsCAACT	GRCh37
NC_000001.9:g.191439429_191439433delinsCAACT	NCBI36
NG_012691.1:g.86719_86723delinsCAACT , LRG_507:g.86719_86723delinsCAACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-119_973-115delinsCAACT MANE Select	ENSP00000356405.4:n.973-119_973-115delinsCAACT
ENST00000635846.1:c.730-119_730-115delinsCAACT	ENSP00000490035.1:n.730-119_730-115delinsCAACT
ENST00000643006.1:c.1041-119_1041-115delinsCAACT	ENSP00000496633.1:n.1041-119_1041-115delinsCAACT
ENST00000648071.1:c.*949-119_*949-115delinsCAACT	ENSP00000497513.1:n.*949-119_*949-115delinsCAACT
ENST00000649613.1:n.223-119_223-115delinsCAACT
ENST00000649895.1:n.1191-119_1191-115delinsCAACT
ENST00000650197.1:c.973-119_973-115delinsCAACT	ENSP00000496929.1:n.973-119_973-115delinsCAACT
ENST00000367435.3:c.973-119_973-115delinsCAACT	ENSP00000356405.3:n.973-119_973-115delinsCAACT
NM_024529.4:c.973-119_973-115delinsCAACT , LRG_507t1:c.973-119_973-115delinsCAACT	NP_078805.3:n.973-119_973-115delinsCAACT
NM_024529.5:c.973-119_973-115delinsCAACT MANE Select	NP_078805.3:n.973-119_973-115delinsCAACT