Canonical Allele Identifier: CA2697564133
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1334391662
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193203856G>A , CM000663.2:g.193203856G>A GRCh38
NC_000001.10:g.193172986G>A , CM000663.1:g.193172986G>A GRCh37
NC_000001.9:g.191439609G>A NCBI36
NG_012691.1:g.86899G>A , LRG_507:g.86899G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367435.5:c.1030+4G>A MANE Select ENSP00000356405.4:n.1030+4G>A
ENST00000635846.1:c.787+4G>A ENSP00000490035.1:n.787+4G>A
ENST00000643006.1:c.1098+4G>A ENSP00000496633.1:n.1098+4G>A
ENST00000648071.1:c.*1006+4G>A ENSP00000497513.1:n.*1006+4G>A
ENST00000649613.1:n.280+4G>A
ENST00000649895.1:n.1248+4G>A
ENST00000650197.1:c.1030+4G>A ENSP00000496929.1:n.1030+4G>A
ENST00000367435.3:c.1030+4G>A ENSP00000356405.3:n.1030+4G>A
NM_024529.4:c.1030+4G>A , LRG_507t1:c.1030+4G>A NP_078805.3:n.1030+4G>A
NM_024529.5:c.1030+4G>A MANE Select NP_078805.3:n.1030+4G>A
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