Canonical Allele Identifier: CA528011324

Gene: CDC73

Linked Data

• dbSNP Id: rs1461231690
• gnomAD v2: 1-193173019-AAAGATCG-A
• gnomAD v3: 1-193203889-AAAGATCG-A
• gnomAD v4: 1-193203889-AAAGATCG-A
• MyVariant Identifiers: chr1:g.193173020_193173026del (hg19) ; chr1:g.193203890_193203896del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193203890_193203896del , CM000663.2:g.193203890_193203896del	GRCh38
NC_000001.10:g.193173020_193173026del , CM000663.1:g.193173020_193173026del	GRCh37
NC_000001.9:g.191439643_191439649del	NCBI36
NG_012691.1:g.86933_86939del , LRG_507:g.86933_86939del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.1030+38_1030+44del MANE Select	ENSP00000356405.4:n.1030+38_1030+44del
ENST00000635846.1:c.787+38_787+44del	ENSP00000490035.1:n.787+38_787+44del
ENST00000643006.1:c.1098+38_1098+44del	ENSP00000496633.1:n.1098+38_1098+44del
ENST00000648071.1:c.*1006+38_*1006+44del	ENSP00000497513.1:n.*1006+38_*1006+44del
ENST00000649613.1:n.280+38_280+44del
ENST00000649895.1:n.1248+38_1248+44del
ENST00000650197.1:c.1030+38_1030+44del	ENSP00000496929.1:n.1030+38_1030+44del
ENST00000367435.3:c.1030+38_1030+44del	ENSP00000356405.3:n.1030+38_1030+44del
NM_024529.4:c.1030+38_1030+44del , LRG_507t1:c.1030+38_1030+44del	NP_078805.3:n.1030+38_1030+44del
NM_024529.5:c.1030+38_1030+44del MANE Select	NP_078805.3:n.1030+38_1030+44del