Canonical Allele Identifier: CA2649598692

Gene: CDC73

Linked Data

• gnomAD v4: 1-193203664-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203664C>T , CM000663.2:g.193203664C>T	GRCh38
NC_000001.10:g.193172794C>T , CM000663.1:g.193172794C>T	GRCh37
NC_000001.9:g.191439417C>T	NCBI36
NG_012691.1:g.86707C>T , LRG_507:g.86707C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.973-131C>T MANE Select	ENSP00000356405.4:n.973-131C>T
ENST00000635846.1:c.730-131C>T	ENSP00000490035.1:n.730-131C>T
ENST00000643006.1:c.1041-131C>T	ENSP00000496633.1:n.1041-131C>T
ENST00000648071.1:c.*949-131C>T	ENSP00000497513.1:n.*949-131C>T
ENST00000649613.1:n.223-131C>T
ENST00000649895.1:n.1191-131C>T
ENST00000650197.1:c.973-131C>T	ENSP00000496929.1:n.973-131C>T
ENST00000367435.3:c.973-131C>T	ENSP00000356405.3:n.973-131C>T
NM_024529.4:c.973-131C>T , LRG_507t1:c.973-131C>T	NP_078805.3:n.973-131C>T
NM_024529.5:c.973-131C>T MANE Select	NP_078805.3:n.973-131C>T