Canonical Allele Identifier: CA422491614

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193172930T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203800T>C , CM000663.2:g.193203800T>C	GRCh38
NC_000001.10:g.193172930T>C , CM000663.1:g.193172930T>C	GRCh37
NC_000001.9:g.191439553T>C	NCBI36
NG_012691.1:g.86843T>C , LRG_507:g.86843T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.978T>C MANE Select	ENSP00000356405.4:p.Gly326=
ENST00000635846.1:c.735T>C	ENSP00000490035.1:p.Gly245=
ENST00000643006.1:c.1046T>C	ENSP00000496633.1:p.Val349Ala
ENST00000648071.1:c.*954T>C	ENSP00000497513.1:n.*954T>C
ENST00000649613.1:n.228T>C
ENST00000649895.1:n.1196T>C
ENST00000650197.1:c.978T>C	ENSP00000496929.1:p.Gly326=
ENST00000367435.3:c.978T>C	ENSP00000356405.3:p.Gly326=
NM_024529.4:c.978T>C , LRG_507t1:c.978T>C	NP_078805.3:p.Gly326=
NM_024529.5:c.978T>C MANE Select	NP_078805.3:p.Gly326=