Canonical Allele Identifier: CA422349265

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193091438G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122308G>T , CM000663.2:g.193122308G>T	GRCh38
NC_000001.10:g.193091438G>T , CM000663.1:g.193091438G>T	GRCh37
NC_000001.9:g.191358061G>T	NCBI36
NG_012691.1:g.5351G>T , LRG_507:g.5351G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.108G>T MANE Select	ENSP00000356405.4:p.Val36=
ENST00000635846.1:c.108G>T	ENSP00000490035.1:p.Val36=
ENST00000643006.1:c.108G>T	ENSP00000496633.1:p.Val36=
ENST00000643784.1:c.108G>T	ENSP00000494944.1:p.Val36=
ENST00000647662.1:n.9G>T
ENST00000648071.1:c.108G>T	ENSP00000497513.1:p.Val36=
ENST00000649606.1:n.121G>T
ENST00000649895.1:n.326G>T
ENST00000650197.1:c.108G>T	ENSP00000496929.1:p.Val36=
ENST00000367435.3:c.108G>T	ENSP00000356405.3:p.Val36=
NM_024529.4:c.108G>T , LRG_507t1:c.108G>T	NP_078805.3:p.Val36=
XM_006711537.2:c.108G>T	XP_006711600.1:p.Val36=
XM_006711537.4:c.108G>T	XP_006711600.1:p.Val36=
XR_001738350.1:n.1349C>A
NM_024529.5:c.108G>T MANE Select	NP_078805.3:p.Val36=