Canonical Allele Identifier: CA1216149983

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203835A= , CM000663.2:g.193203835A=	GRCh38
NC_000001.10:g.193172965A= , CM000663.1:g.193172965A=	GRCh37
NC_000001.9:g.191439588A=	NCBI36
NG_012691.1:g.86878A= , LRG_507:g.86878A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1013A= MANE Select	ENSP00000356405.4:p.Gln338=
ENST00000635846.1:c.770A=	ENSP00000490035.1:p.Gln257=
ENST00000643006.1:c.1081A=	ENSP00000496633.1:p.Ser361=
ENST00000648071.1:c.*989A=	ENSP00000497513.1:n.*989A=
ENST00000649613.1:n.263A=
ENST00000649895.1:n.1231A=
ENST00000650197.1:c.1013A=	ENSP00000496929.1:p.Gln338=
ENST00000367435.3:c.1013A=	ENSP00000356405.3:p.Gln338=
NM_024529.4:c.1013A= , LRG_507t1:c.1013A=	NP_078805.3:p.Gln338=
NM_024529.5:c.1013A= MANE Select	NP_078805.3:p.Gln338=