Canonical Allele Identifier: CA528080303

Gene: CDC73

Linked Data

• dbSNP Id: rs1558285057
• gnomAD v2: 1-193111216-C-CA
• gnomAD v4: 1-193142086-C-CA
• MyVariant Identifiers: chr1:g.193111216_193111217insA (hg19) ; chr1:g.193142086_193142087insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142087dup , CM000663.2:g.193142087dup	GRCh38
NC_000001.10:g.193111217dup , CM000663.1:g.193111217dup	GRCh37
NC_000001.9:g.191377840dup	NCBI36
NG_012691.1:g.25130dup , LRG_507:g.25130dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.729+21dup MANE Select	ENSP00000356405.4:n.729+21dup
ENST00000635846.1:c.729+21dup	ENSP00000490035.1:n.729+21dup
ENST00000643006.1:c.729+21dup	ENSP00000496633.1:n.729+21dup
ENST00000643784.1:c.*205+21dup	ENSP00000494944.1:n.*205+21dup
ENST00000647662.1:n.630+21dup
ENST00000648071.1:c.*705+21dup	ENSP00000497513.1:n.*705+21dup
ENST00000649606.1:n.742+21dup
ENST00000649895.1:n.947+21dup
ENST00000650197.1:c.729+21dup	ENSP00000496929.1:n.729+21dup
ENST00000367435.3:c.729+21dup	ENSP00000356405.3:n.729+21dup
NM_024529.4:c.729+21dup , LRG_507t1:c.729+21dup	NP_078805.3:n.729+21dup
XM_006711537.2:c.729+21dup	XP_006711600.1:n.729+21dup
XM_006711537.4:c.729+21dup	XP_006711600.1:n.729+21dup
NM_024529.5:c.729+21dup MANE Select	NP_078805.3:n.729+21dup