Canonical Allele Identifier: CA1216117034

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193130109T= , CM000663.2:g.193130109T=	GRCh38
NC_000001.10:g.193099239T= , CM000663.1:g.193099239T=	GRCh37
NC_000001.9:g.191365862T=	NCBI36
NG_012691.1:g.13152T= , LRG_507:g.13152T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367435.5:c.238-65T= MANE Select	ENSP00000356405.4:n.238-65T=
ENST00000635846.1:c.238-65T=	ENSP00000490035.1:n.238-65T=
ENST00000643006.1:c.238-65T=	ENSP00000496633.1:n.238-65T=
ENST00000643784.1:c.238-65T=	ENSP00000494944.1:n.238-65T=
ENST00000647662.1:n.139-65T=
ENST00000648071.1:c.*214-65T=	ENSP00000497513.1:n.*214-65T=
ENST00000649606.1:n.251-65T=
ENST00000649706.1:n.179-65T=
ENST00000649895.1:n.456-65T=
ENST00000650197.1:c.238-65T=	ENSP00000496929.1:n.238-65T=
ENST00000367435.3:c.238-65T=	ENSP00000356405.3:n.238-65T=
ENST00000482484.1:n.490-65T=
NM_024529.4:c.238-65T= , LRG_507t1:c.238-65T=	NP_078805.3:n.238-65T=
XM_006711537.2:c.238-65T=	XP_006711600.1:n.238-65T=
XR_241165.2:n.303+248A=
XM_006711537.4:c.238-65T=	XP_006711600.1:n.238-65T=
NM_024529.5:c.238-65T= MANE Select	NP_078805.3:n.238-65T=