Canonical Allele Identifier: CA2649626080

Gene: CDC73

Linked Data

• dbSNP Id: rs1675668543
• gnomAD v4: 1-193130104-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193130104C>T , CM000663.2:g.193130104C>T	GRCh38
NC_000001.10:g.193099234C>T , CM000663.1:g.193099234C>T	GRCh37
NC_000001.9:g.191365857C>T	NCBI36
NG_012691.1:g.13147C>T , LRG_507:g.13147C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367435.5:c.238-70C>T MANE Select	ENSP00000356405.4:n.238-70C>T
ENST00000635846.1:c.238-70C>T	ENSP00000490035.1:n.238-70C>T
ENST00000643006.1:c.238-70C>T	ENSP00000496633.1:n.238-70C>T
ENST00000643784.1:c.238-70C>T	ENSP00000494944.1:n.238-70C>T
ENST00000647662.1:n.139-70C>T
ENST00000648071.1:c.*214-70C>T	ENSP00000497513.1:n.*214-70C>T
ENST00000649606.1:n.251-70C>T
ENST00000649706.1:n.179-70C>T
ENST00000649895.1:n.456-70C>T
ENST00000650197.1:c.238-70C>T	ENSP00000496929.1:n.238-70C>T
ENST00000367435.3:c.238-70C>T	ENSP00000356405.3:n.238-70C>T
ENST00000482484.1:n.490-70C>T
NM_024529.4:c.238-70C>T , LRG_507t1:c.238-70C>T	NP_078805.3:n.238-70C>T
XM_006711537.2:c.238-70C>T	XP_006711600.1:n.238-70C>T
XR_241165.2:n.303+253G>A
XM_006711537.4:c.238-70C>T	XP_006711600.1:n.238-70C>T
NM_024529.5:c.238-70C>T MANE Select	NP_078805.3:n.238-70C>T