Canonical Allele Identifier: CA2649626078

Gene: CDC73

Linked Data

• gnomAD v4: 1-193130101-TTAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193130102_193130104del , CM000663.2:g.193130102_193130104del	GRCh38
NC_000001.10:g.193099232_193099234del , CM000663.1:g.193099232_193099234del	GRCh37
NC_000001.9:g.191365855_191365857del	NCBI36
NG_012691.1:g.13145_13147del , LRG_507:g.13145_13147del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367435.5:c.238-72_238-70del MANE Select	ENSP00000356405.4:n.238-72_238-70del
ENST00000635846.1:c.238-72_238-70del	ENSP00000490035.1:n.238-72_238-70del
ENST00000643006.1:c.238-72_238-70del	ENSP00000496633.1:n.238-72_238-70del
ENST00000643784.1:c.238-72_238-70del	ENSP00000494944.1:n.238-72_238-70del
ENST00000647662.1:n.139-72_139-70del
ENST00000648071.1:c.*214-72_*214-70del	ENSP00000497513.1:n.*214-72_*214-70del
ENST00000649606.1:n.251-72_251-70del
ENST00000649706.1:n.179-72_179-70del
ENST00000649895.1:n.456-72_456-70del
ENST00000650197.1:c.238-72_238-70del	ENSP00000496929.1:n.238-72_238-70del
ENST00000367435.3:c.238-72_238-70del	ENSP00000356405.3:n.238-72_238-70del
ENST00000482484.1:n.490-72_490-70del
NM_024529.4:c.238-72_238-70del , LRG_507t1:c.238-72_238-70del	NP_078805.3:n.238-72_238-70del
XM_006711537.2:c.238-72_238-70del	XP_006711600.1:n.238-72_238-70del
XR_241165.2:n.303+253_303+255del
XM_006711537.4:c.238-72_238-70del	XP_006711600.1:n.238-72_238-70del
NM_024529.5:c.238-72_238-70del MANE Select	NP_078805.3:n.238-72_238-70del