Canonical Allele Identifier: CA344078485

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193218925A>C (hg19) ; chr1:g.193249795A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193249795A>C , CM000663.2:g.193249795A>C	GRCh38
NC_000001.10:g.193218925A>C , CM000663.1:g.193218925A>C	GRCh37
NC_000001.9:g.191485548A>C	NCBI36
NG_012691.1:g.132838A>C , LRG_507:g.132838A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1483A>C MANE Select	ENSP00000356405.4:p.Thr495Pro
ENST00000635846.1:c.1240A>C	ENSP00000490035.1:p.Thr414Pro
ENST00000643006.1:c.*393A>C	ENSP00000496633.1:n.*393A>C
ENST00000648071.1:c.*1459A>C	ENSP00000497513.1:n.*1459A>C
ENST00000649613.1:n.733A>C
ENST00000650197.1:c.*181A>C	ENSP00000496929.1:n.*181A>C
ENST00000367435.3:c.1483A>C	ENSP00000356405.3:p.Thr495Pro
ENST00000477868.1:n.195A>C
NM_024529.4:c.1483A>C , LRG_507t1:c.1483A>C	NP_078805.3:p.Thr495Pro
NM_024529.5:c.1483A>C MANE Select	NP_078805.3:p.Thr495Pro