Canonical Allele Identifier: CA343961158

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193107250G>T (hg19) ; chr1:g.193138120G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193138120G>T , CM000663.2:g.193138120G>T	GRCh38
NC_000001.10:g.193107250G>T , CM000663.1:g.193107250G>T	GRCh37
NC_000001.9:g.191373873G>T	NCBI36
NG_012691.1:g.21163G>T , LRG_507:g.21163G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367435.5:c.459G>T MANE Select	ENSP00000356405.4:p.Leu153Phe
ENST00000635846.1:c.459G>T	ENSP00000490035.1:p.Leu153Phe
ENST00000643006.1:c.459G>T	ENSP00000496633.1:p.Leu153Phe
ENST00000643784.1:c.459G>T	ENSP00000494944.1:p.Leu153Phe
ENST00000647662.1:n.360G>T
ENST00000648071.1:c.*435G>T	ENSP00000497513.1:n.*435G>T
ENST00000649606.1:n.472G>T
ENST00000649706.1:n.400G>T
ENST00000649895.1:n.677G>T
ENST00000650197.1:c.459G>T	ENSP00000496929.1:p.Leu153Phe
ENST00000367435.3:c.459G>T	ENSP00000356405.3:p.Leu153Phe
ENST00000482484.1:n.711G>T
NM_024529.4:c.459G>T , LRG_507t1:c.459G>T	NP_078805.3:p.Leu153Phe
XM_006711537.2:c.459G>T	XP_006711600.1:p.Leu153Phe
XM_006711537.4:c.459G>T	XP_006711600.1:p.Leu153Phe
NM_024529.5:c.459G>T MANE Select	NP_078805.3:p.Leu153Phe