Canonical Allele Identifier: CA1303711

Gene: CDC73

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203831G>A , CM000663.2:g.193203831G>A	GRCh38
NC_000001.10:g.193172961G>A , CM000663.1:g.193172961G>A	GRCh37
NC_000001.9:g.191439584G>A	NCBI36
NG_012691.1:g.86874G>A , LRG_507:g.86874G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024529.5:c.1009G>A MANE Select	NP_078805.3:p.Ala337Thr
ENST00000367435.5:c.1009G>A MANE Select	ENSP00000356405.4:p.Ala337Thr
NM_024529.4:c.1009G>A , LRG_507t1:c.1009G>A	NP_078805.3:p.Ala337Thr
ENST00000367435.3:c.1009G>A	ENSP00000356405.3:p.Ala337Thr
ENST00000635846.1:c.766G>A	ENSP00000490035.1:p.Ala256Thr
ENST00000643006.1:c.1077G>A	ENSP00000496633.1:p.Gln359=
ENST00000648071.1:c.*985G>A	ENSP00000497513.1:n.*985G>A
ENST00000649613.1:n.259G>A
ENST00000649895.1:n.1227G>A
ENST00000650197.1:c.1009G>A	ENSP00000496929.1:p.Ala337Thr