Canonical Allele Identifier: CA343962447

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193111063C>T (hg19) ; chr1:g.193141933C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193141933C>T , CM000663.2:g.193141933C>T	GRCh38
NC_000001.10:g.193111063C>T , CM000663.1:g.193111063C>T	GRCh37
NC_000001.9:g.191377686C>T	NCBI36
NG_012691.1:g.24976C>T , LRG_507:g.24976C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.596C>T MANE Select	ENSP00000356405.4:p.Thr199Ile
ENST00000635846.1:c.596C>T	ENSP00000490035.1:p.Thr199Ile
ENST00000643006.1:c.596C>T	ENSP00000496633.1:p.Thr199Ile
ENST00000643784.1:c.*72C>T	ENSP00000494944.1:n.*72C>T
ENST00000647662.1:n.497C>T
ENST00000648071.1:c.*572C>T	ENSP00000497513.1:n.*572C>T
ENST00000649606.1:n.609C>T
ENST00000649706.1:n.537C>T
ENST00000649895.1:n.814C>T
ENST00000650197.1:c.596C>T	ENSP00000496929.1:p.Thr199Ile
ENST00000367435.3:c.596C>T	ENSP00000356405.3:p.Thr199Ile
NM_024529.4:c.596C>T , LRG_507t1:c.596C>T	NP_078805.3:p.Thr199Ile
XM_006711537.2:c.596C>T	XP_006711600.1:p.Thr199Ile
XM_006711537.4:c.596C>T	XP_006711600.1:p.Thr199Ile
NM_024529.5:c.596C>T MANE Select	NP_078805.3:p.Thr199Ile