Canonical Allele Identifier: CA916368801

Gene: CDC73

Linked Data

• dbSNP Id: rs1572139462
• gnomAD v3: 1-193122103-AAGG-A
• gnomAD v4: 1-193122103-AAGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193122114_193122116del , CM000663.2:g.193122114_193122116del	GRCh38
NC_000001.10:g.193091244_193091246del , CM000663.1:g.193091244_193091246del	GRCh37
NC_000001.9:g.191357867_191357869del	NCBI36
NG_012691.1:g.5157_5159del , LRG_507:g.5157_5159del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.-87_-85del MANE Select	ENSP00000356405.4:n.-87_-85del
ENST00000643006.1:c.-87_-85del	ENSP00000496633.1:n.-87_-85del
ENST00000649895.1:n.132_134del
ENST00000650197.1:c.-87_-85del	ENSP00000496929.1:n.-87_-85del
ENST00000367435.3:c.-87_-85del	ENSP00000356405.3:n.-87_-85del
NM_024529.4:c.-87_-85del , LRG_507t1:c.-87_-85del	NP_078805.3:n.-87_-85del
XM_006711537.2:c.-87_-85del	XP_006711600.1:n.-87_-85del
XM_006711537.4:c.-87_-85del	XP_006711600.1:n.-87_-85del
XR_001738350.1:n.1551_1553del
NM_024529.5:c.-87_-85del MANE Select	NP_078805.3:n.-87_-85del