Canonical Allele Identifier: CA1010623014
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs776686364

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203709_193203712del , CM000663.2:g.193203709_193203712del GRCh38
NC_000001.10:g.193172839_193172842del , CM000663.1:g.193172839_193172842del GRCh37
NC_000001.9:g.191439462_191439465del NCBI36
NG_012691.1:g.86752_86755del , LRG_507:g.86752_86755del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.973-86_973-83del MANE Select ENSP00000356405.4:n.973-86_973-83del
ENST00000635846.1:c.730-86_730-83del ENSP00000490035.1:n.730-86_730-83del
ENST00000643006.1:c.1041-86_1041-83del ENSP00000496633.1:n.1041-86_1041-83del
ENST00000648071.1:c.*949-86_*949-83del ENSP00000497513.1:n.*949-86_*949-83del
ENST00000649613.1:n.223-86_223-83del
ENST00000649895.1:n.1191-86_1191-83del
ENST00000650197.1:c.973-86_973-83del ENSP00000496929.1:n.973-86_973-83del
ENST00000367435.3:c.973-86_973-83del ENSP00000356405.3:n.973-86_973-83del
NM_024529.4:c.973-86_973-83del , LRG_507t1:c.973-86_973-83del NP_078805.3:n.973-86_973-83del
NM_024529.5:c.973-86_973-83del MANE Select NP_078805.3:n.973-86_973-83del