Canonical Allele Identifier: CA344076128

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193172950A>T (hg19) ; chr1:g.193203820A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203820A>T , CM000663.2:g.193203820A>T	GRCh38
NC_000001.10:g.193172950A>T , CM000663.1:g.193172950A>T	GRCh37
NC_000001.9:g.191439573A>T	NCBI36
NG_012691.1:g.86863A>T , LRG_507:g.86863A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.998A>T MANE Select	ENSP00000356405.4:p.Gln333Leu
ENST00000635846.1:c.755A>T	ENSP00000490035.1:p.Gln252Leu
ENST00000643006.1:c.1066A>T	ENSP00000496633.1:p.Arg356Ter
ENST00000648071.1:c.*974A>T	ENSP00000497513.1:n.*974A>T
ENST00000649613.1:n.248A>T
ENST00000649895.1:n.1216A>T
ENST00000650197.1:c.998A>T	ENSP00000496929.1:p.Gln333Leu
ENST00000367435.3:c.998A>T	ENSP00000356405.3:p.Gln333Leu
NM_024529.4:c.998A>T , LRG_507t1:c.998A>T	NP_078805.3:p.Gln333Leu
NM_024529.5:c.998A>T MANE Select	NP_078805.3:p.Gln333Leu