Canonical Allele Identifier: CA422348741

Gene: CDC73

Linked Data

• dbSNP Id: rs1675464727
• gnomAD v4: 1-193122257-G-A
• MyVariant Identifiers: chr1:g.193091387G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122257G>A , CM000663.2:g.193122257G>A	GRCh38
NC_000001.10:g.193091387G>A , CM000663.1:g.193091387G>A	GRCh37
NC_000001.9:g.191358010G>A	NCBI36
NG_012691.1:g.5300G>A , LRG_507:g.5300G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.57G>A MANE Select	ENSP00000356405.4:p.Val19=
ENST00000635846.1:c.57G>A	ENSP00000490035.1:p.Val19=
ENST00000643006.1:c.57G>A	ENSP00000496633.1:p.Val19=
ENST00000643784.1:c.57G>A	ENSP00000494944.1:p.Val19=
ENST00000648071.1:c.57G>A	ENSP00000497513.1:p.Val19=
ENST00000649606.1:n.70G>A
ENST00000649895.1:n.275G>A
ENST00000650197.1:c.57G>A	ENSP00000496929.1:p.Val19=
ENST00000367435.3:c.57G>A	ENSP00000356405.3:p.Val19=
NM_024529.4:c.57G>A , LRG_507t1:c.57G>A	NP_078805.3:p.Val19=
XM_006711537.2:c.57G>A	XP_006711600.1:p.Val19=
XM_006711537.4:c.57G>A	XP_006711600.1:p.Val19=
XR_001738350.1:n.1400C>T
NM_024529.5:c.57G>A MANE Select	NP_078805.3:p.Val19=