Canonical Allele Identifier: CA729344021
Gene: CDC73 HGNC NCBI

Linked Data

dbSNP Id: rs1338058790
MyVariant Identifiers: chr1:g.193091245G>A (hg19) chr1:g.193122115G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193122115G>A , CM000663.2:g.193122115G>A GRCh38
NC_000001.10:g.193091245G>A , CM000663.1:g.193091245G>A GRCh37
NC_000001.9:g.191357868G>A NCBI36
NG_012691.1:g.5158G>A , LRG_507:g.5158G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367435.5:c.-86G>A MANE Select ENSP00000356405.4:n.-86G>A
ENST00000643006.1:c.-86G>A ENSP00000496633.1:n.-86G>A
ENST00000649895.1:n.133G>A
ENST00000650197.1:c.-86G>A ENSP00000496929.1:n.-86G>A
ENST00000367435.3:c.-86G>A ENSP00000356405.3:n.-86G>A
NM_024529.4:c.-86G>A , LRG_507t1:c.-86G>A NP_078805.3:n.-86G>A
XM_006711537.2:c.-86G>A XP_006711600.1:n.-86G>A
XM_006711537.4:c.-86G>A XP_006711600.1:n.-86G>A
XR_001738350.1:n.1542C>T
NM_024529.5:c.-86G>A MANE Select NP_078805.3:n.-86G>A
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