Canonical Allele Identifier: CA343964144

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193147939C>T , CM000663.2:g.193147939C>T	GRCh38
NC_000001.10:g.193117069C>T , CM000663.1:g.193117069C>T	GRCh37
NC_000001.9:g.191383692C>T	NCBI36
NG_012691.1:g.30982C>T , LRG_507:g.30982C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.802C>T MANE Select	NP_078805.3:p.Arg268Ter
ENST00000367435.5:c.802C>T MANE Select	ENSP00000356405.4:p.Arg268Ter
NM_024529.4:c.802C>T , LRG_507t1:c.802C>T	NP_078805.3:p.Arg268Ter
ENST00000367435.3:c.802C>T	ENSP00000356405.3:p.Arg268Ter
ENST00000635846.1:c.729+5873C>T	ENSP00000490035.1:n.729+5873C>T
ENST00000643006.1:c.802C>T	ENSP00000496633.1:p.Arg268Ter
ENST00000643784.1:c.*278C>T	ENSP00000494944.1:n.*278C>T
ENST00000647662.1:n.703C>T
ENST00000648071.1:c.*778C>T	ENSP00000497513.1:n.*778C>T
ENST00000649606.1:n.815C>T
ENST00000649895.1:n.1020C>T
ENST00000650197.1:c.802C>T	ENSP00000496929.1:p.Arg268Ter
XM_006711537.2:c.802C>T	XP_006711600.1:p.Arg268Ter
XM_006711537.4:c.802C>T	XP_006711600.1:p.Arg268Ter