Canonical Allele Identifier: CA343973371

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193130220T>C , CM000663.2:g.193130220T>C	GRCh38
NC_000001.10:g.193099350T>C , CM000663.1:g.193099350T>C	GRCh37
NC_000001.9:g.191365973T>C	NCBI36
NG_012691.1:g.13263T>C , LRG_507:g.13263T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.284T>C MANE Select	NP_078805.3:p.Leu95Pro
ENST00000367435.5:c.284T>C MANE Select	ENSP00000356405.4:p.Leu95Pro
NM_024529.4:c.284T>C , LRG_507t1:c.284T>C	NP_078805.3:p.Leu95Pro
ENST00000367435.3:c.284T>C	ENSP00000356405.3:p.Leu95Pro
ENST00000482484.1:n.536T>C
ENST00000635846.1:c.284T>C	ENSP00000490035.1:p.Leu95Pro
ENST00000643006.1:c.284T>C	ENSP00000496633.1:p.Leu95Pro
ENST00000643784.1:c.284T>C	ENSP00000494944.1:p.Leu95Pro
ENST00000647662.1:n.185T>C
ENST00000648071.1:c.*260T>C	ENSP00000497513.1:n.*260T>C
ENST00000649606.1:n.297T>C
ENST00000649706.1:n.225T>C
ENST00000649895.1:n.502T>C
ENST00000650197.1:c.284T>C	ENSP00000496929.1:p.Leu95Pro
XM_006711537.2:c.284T>C	XP_006711600.1:p.Leu95Pro
XM_006711537.4:c.284T>C	XP_006711600.1:p.Leu95Pro
XR_241165.2:n.303+137A>G