Canonical Allele Identifier: CA729298261

Gene: CDC73

Linked Data

• dbSNP Id: rs1479935376
• gnomAD v3: 1-193203676-C-CA
• gnomAD v4: 1-193203676-C-CA
• MyVariant Identifiers: chr1:g.193172806_193172807insA (hg19) ; chr1:g.193203676_193203677insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203678dup , CM000663.2:g.193203678dup	GRCh38
NC_000001.10:g.193172808dup , CM000663.1:g.193172808dup	GRCh37
NC_000001.9:g.191439431dup	NCBI36
NG_012691.1:g.86721dup , LRG_507:g.86721dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-117dup MANE Select	ENSP00000356405.4:n.973-117dup
ENST00000635846.1:c.730-117dup	ENSP00000490035.1:n.730-117dup
ENST00000643006.1:c.1041-117dup	ENSP00000496633.1:n.1041-117dup
ENST00000648071.1:c.*949-117dup	ENSP00000497513.1:n.*949-117dup
ENST00000649613.1:n.223-117dup
ENST00000649895.1:n.1191-117dup
ENST00000650197.1:c.973-117dup	ENSP00000496929.1:n.973-117dup
ENST00000367435.3:c.973-117dup	ENSP00000356405.3:n.973-117dup
NM_024529.4:c.973-117dup , LRG_507t1:c.973-117dup	NP_078805.3:n.973-117dup
NM_024529.5:c.973-117dup MANE Select	NP_078805.3:n.973-117dup