Canonical Allele Identifier: CA1303447
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs80356646

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193142110_193142117del , CM000663.2:g.193142110_193142117del GRCh38
NC_000001.10:g.193111240_193111247del , CM000663.1:g.193111240_193111247del GRCh37
NC_000001.9:g.191377863_191377870del NCBI36
NG_012691.1:g.25153_25160del , LRG_507:g.25153_25160del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.729+44_729+51del MANE Select ENSP00000356405.4:n.729+44_729+51del
ENST00000635846.1:c.729+44_729+51del ENSP00000490035.1:n.729+44_729+51del
ENST00000643006.1:c.729+44_729+51del ENSP00000496633.1:n.729+44_729+51del
ENST00000643784.1:c.*205+44_*205+51del ENSP00000494944.1:n.*205+44_*205+51del
ENST00000647662.1:n.630+44_630+51del
ENST00000648071.1:c.*705+44_*705+51del ENSP00000497513.1:n.*705+44_*705+51del
ENST00000649606.1:n.742+44_742+51del
ENST00000649895.1:n.947+44_947+51del
ENST00000650197.1:c.729+44_729+51del ENSP00000496929.1:n.729+44_729+51del
ENST00000367435.3:c.729+44_729+51del ENSP00000356405.3:n.729+44_729+51del
NM_024529.4:c.729+44_729+51del , LRG_507t1:c.729+44_729+51del NP_078805.3:n.729+44_729+51del
XM_006711537.2:c.729+44_729+51del XP_006711600.1:n.729+44_729+51del
XM_006711537.4:c.729+44_729+51del XP_006711600.1:n.729+44_729+51del
NM_024529.5:c.729+44_729+51del MANE Select NP_078805.3:n.729+44_729+51del