Canonical Allele Identifier: CA343960775

Gene: CDC73

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193135581C>T , CM000663.2:g.193135581C>T	GRCh38
NC_000001.10:g.193104711C>T , CM000663.1:g.193104711C>T	GRCh37
NC_000001.9:g.191371334C>T	NCBI36
NG_012691.1:g.18624C>T , LRG_507:g.18624C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.415C>T MANE Select	ENSP00000356405.4:p.Arg139Ter
ENST00000635846.1:c.415C>T	ENSP00000490035.1:p.Arg139Ter
ENST00000643006.1:c.415C>T	ENSP00000496633.1:p.Arg139Ter
ENST00000643784.1:c.415C>T	ENSP00000494944.1:p.Arg139Ter
ENST00000647662.1:n.316C>T
ENST00000648071.1:c.*391C>T	ENSP00000497513.1:n.*391C>T
ENST00000649606.1:n.428C>T
ENST00000649706.1:n.356C>T
ENST00000649895.1:n.633C>T
ENST00000650197.1:c.415C>T	ENSP00000496929.1:p.Arg139Ter
ENST00000367435.3:c.415C>T	ENSP00000356405.3:p.Arg139Ter
ENST00000482484.1:n.667C>T
NM_024529.4:c.415C>T , LRG_507t1:c.415C>T	NP_078805.3:p.Arg139Ter
XM_006711537.2:c.415C>T	XP_006711600.1:p.Arg139Ter
XM_006711537.4:c.415C>T	XP_006711600.1:p.Arg139Ter
NM_024529.5:c.415C>T MANE Select	NP_078805.3:p.Arg139Ter