Canonical Allele Identifier: CA2649597936

Gene: CDC73

Linked Data

• gnomAD v4: 1-193142098-T-TGAGAGAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142110_193142117dup , CM000663.2:g.193142110_193142117dup	GRCh38
NC_000001.10:g.193111240_193111247dup , CM000663.1:g.193111240_193111247dup	GRCh37
NC_000001.9:g.191377863_191377870dup	NCBI36
NG_012691.1:g.25153_25160dup , LRG_507:g.25153_25160dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.729+44_729+51dup MANE Select	ENSP00000356405.4:n.729+44_729+51dup
ENST00000635846.1:c.729+44_729+51dup	ENSP00000490035.1:n.729+44_729+51dup
ENST00000643006.1:c.729+44_729+51dup	ENSP00000496633.1:n.729+44_729+51dup
ENST00000643784.1:c.*205+44_*205+51dup	ENSP00000494944.1:n.*205+44_*205+51dup
ENST00000647662.1:n.630+44_630+51dup
ENST00000648071.1:c.*705+44_*705+51dup	ENSP00000497513.1:n.*705+44_*705+51dup
ENST00000649606.1:n.742+44_742+51dup
ENST00000649895.1:n.947+44_947+51dup
ENST00000650197.1:c.729+44_729+51dup	ENSP00000496929.1:n.729+44_729+51dup
ENST00000367435.3:c.729+44_729+51dup	ENSP00000356405.3:n.729+44_729+51dup
NM_024529.4:c.729+44_729+51dup , LRG_507t1:c.729+44_729+51dup	NP_078805.3:n.729+44_729+51dup
XM_006711537.2:c.729+44_729+51dup	XP_006711600.1:n.729+44_729+51dup
XM_006711537.4:c.729+44_729+51dup	XP_006711600.1:n.729+44_729+51dup
NM_024529.5:c.729+44_729+51dup MANE Select	NP_078805.3:n.729+44_729+51dup