Canonical Allele Identifier: CA729344037

Gene: CDC73

Linked Data

• dbSNP Id: rs1415452116
• gnomAD v3: 1-193122124-G-A
• gnomAD v4: 1-193122124-G-A
• MyVariant Identifiers: chr1:g.193091254G>A (hg19) ; chr1:g.193122124G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122124G>A , CM000663.2:g.193122124G>A	GRCh38
NC_000001.10:g.193091254G>A , CM000663.1:g.193091254G>A	GRCh37
NC_000001.9:g.191357877G>A	NCBI36
NG_012691.1:g.5167G>A , LRG_507:g.5167G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-77G>A MANE Select	ENSP00000356405.4:n.-77G>A
ENST00000643006.1:c.-77G>A	ENSP00000496633.1:n.-77G>A
ENST00000643784.1:c.-77G>A	ENSP00000494944.1:n.-77G>A
ENST00000649895.1:n.142G>A
ENST00000650197.1:c.-77G>A	ENSP00000496929.1:n.-77G>A
ENST00000367435.3:c.-77G>A	ENSP00000356405.3:n.-77G>A
NM_024529.4:c.-77G>A , LRG_507t1:c.-77G>A	NP_078805.3:n.-77G>A
XM_006711537.2:c.-77G>A	XP_006711600.1:n.-77G>A
XM_006711537.4:c.-77G>A	XP_006711600.1:n.-77G>A
XR_001738350.1:n.1533C>T
NM_024529.5:c.-77G>A MANE Select	NP_078805.3:n.-77G>A