Canonical Allele Identifier: CA343961171

Gene: CDC73

Linked Data

• dbSNP Id: rs1675832750
• gnomAD v3: 1-193138122-C-T
• gnomAD v4: 1-193138122-C-T
• MyVariant Identifiers: chr1:g.193107252C>T (hg19) ; chr1:g.193138122C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193138122C>T , CM000663.2:g.193138122C>T	GRCh38
NC_000001.10:g.193107252C>T , CM000663.1:g.193107252C>T	GRCh37
NC_000001.9:g.191373875C>T	NCBI36
NG_012691.1:g.21165C>T , LRG_507:g.21165C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367435.5:c.461C>T MANE Select	ENSP00000356405.4:p.Ala154Val
ENST00000635846.1:c.461C>T	ENSP00000490035.1:p.Ala154Val
ENST00000643006.1:c.461C>T	ENSP00000496633.1:p.Ala154Val
ENST00000643784.1:c.461C>T	ENSP00000494944.1:p.Ala154Val
ENST00000647662.1:n.362C>T
ENST00000648071.1:c.*437C>T	ENSP00000497513.1:n.*437C>T
ENST00000649606.1:n.474C>T
ENST00000649706.1:n.402C>T
ENST00000649895.1:n.679C>T
ENST00000650197.1:c.461C>T	ENSP00000496929.1:p.Ala154Val
ENST00000367435.3:c.461C>T	ENSP00000356405.3:p.Ala154Val
ENST00000482484.1:n.713C>T
NM_024529.4:c.461C>T , LRG_507t1:c.461C>T	NP_078805.3:p.Ala154Val
XM_006711537.2:c.461C>T	XP_006711600.1:p.Ala154Val
XM_006711537.4:c.461C>T	XP_006711600.1:p.Ala154Val
NM_024529.5:c.461C>T MANE Select	NP_078805.3:p.Ala154Val