Canonical Allele Identifier: CA344076111

Gene: CDC73

Linked Data

• MyVariant Identifiers: chr1:g.193172943A>T (hg19) ; chr1:g.193203813A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203813A>T , CM000663.2:g.193203813A>T	GRCh38
NC_000001.10:g.193172943A>T , CM000663.1:g.193172943A>T	GRCh37
NC_000001.9:g.191439566A>T	NCBI36
NG_012691.1:g.86856A>T , LRG_507:g.86856A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.991A>T MANE Select	ENSP00000356405.4:p.Lys331Ter
ENST00000635846.1:c.748A>T	ENSP00000490035.1:p.Lys250Ter
ENST00000643006.1:c.1059A>T	ENSP00000496633.1:p.Gly353=
ENST00000648071.1:c.*967A>T	ENSP00000497513.1:n.*967A>T
ENST00000649613.1:n.241A>T
ENST00000649895.1:n.1209A>T
ENST00000650197.1:c.991A>T	ENSP00000496929.1:p.Lys331Ter
ENST00000367435.3:c.991A>T	ENSP00000356405.3:p.Lys331Ter
NM_024529.4:c.991A>T , LRG_507t1:c.991A>T	NP_078805.3:p.Lys331Ter
NM_024529.5:c.991A>T MANE Select	NP_078805.3:p.Lys331Ter