Canonical Allele Identifier: CA1216149920

Gene: CDC73

Linked Data

• dbSNP Id: rs1677129136
• gnomAD v4: 1-193203662-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203662T>A , CM000663.2:g.193203662T>A	GRCh38
NC_000001.10:g.193172792T>A , CM000663.1:g.193172792T>A	GRCh37
NC_000001.9:g.191439415T>A	NCBI36
NG_012691.1:g.86705T>A , LRG_507:g.86705T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-133T>A MANE Select	ENSP00000356405.4:n.973-133T>A
ENST00000635846.1:c.730-133T>A	ENSP00000490035.1:n.730-133T>A
ENST00000643006.1:c.1041-133T>A	ENSP00000496633.1:n.1041-133T>A
ENST00000648071.1:c.*949-133T>A	ENSP00000497513.1:n.*949-133T>A
ENST00000649613.1:n.223-133T>A
ENST00000649895.1:n.1191-133T>A
ENST00000650197.1:c.973-133T>A	ENSP00000496929.1:n.973-133T>A
ENST00000367435.3:c.973-133T>A	ENSP00000356405.3:n.973-133T>A
NM_024529.4:c.973-133T>A , LRG_507t1:c.973-133T>A	NP_078805.3:n.973-133T>A
NM_024529.5:c.973-133T>A MANE Select	NP_078805.3:n.973-133T>A