Canonical Allele Identifier: CA2649597928

Gene: CDC73

Linked Data

• gnomAD v4: 1-193142094-GGAGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142098_193142101del , CM000663.2:g.193142098_193142101del	GRCh38
NC_000001.10:g.193111228_193111231del , CM000663.1:g.193111228_193111231del	GRCh37
NC_000001.9:g.191377851_191377854del	NCBI36
NG_012691.1:g.25141_25144del , LRG_507:g.25141_25144del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.729+32_729+35del MANE Select	ENSP00000356405.4:n.729+32_729+35del
ENST00000635846.1:c.729+32_729+35del	ENSP00000490035.1:n.729+32_729+35del
ENST00000643006.1:c.729+32_729+35del	ENSP00000496633.1:n.729+32_729+35del
ENST00000643784.1:c.*205+32_*205+35del	ENSP00000494944.1:n.*205+32_*205+35del
ENST00000647662.1:n.630+32_630+35del
ENST00000648071.1:c.*705+32_*705+35del	ENSP00000497513.1:n.*705+32_*705+35del
ENST00000649606.1:n.742+32_742+35del
ENST00000649895.1:n.947+32_947+35del
ENST00000650197.1:c.729+32_729+35del	ENSP00000496929.1:n.729+32_729+35del
ENST00000367435.3:c.729+32_729+35del	ENSP00000356405.3:n.729+32_729+35del
NM_024529.4:c.729+32_729+35del , LRG_507t1:c.729+32_729+35del	NP_078805.3:n.729+32_729+35del
XM_006711537.2:c.729+32_729+35del	XP_006711600.1:n.729+32_729+35del
XM_006711537.4:c.729+32_729+35del	XP_006711600.1:n.729+32_729+35del
NM_024529.5:c.729+32_729+35del MANE Select	NP_078805.3:n.729+32_729+35del