Canonical Allele Identifier: CA2697545681

Gene: CDC73

Linked Data

• dbSNP Id: rs1254750614

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193142106_193142107insCA , CM000663.2:g.193142106_193142107insCA	GRCh38
NC_000001.10:g.193111236_193111237insCA , CM000663.1:g.193111236_193111237insCA	GRCh37
NC_000001.9:g.191377859_191377860insCA	NCBI36
NG_012691.1:g.25149_25150insCA , LRG_507:g.25149_25150insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367435.5:c.729+40_729+41insCA MANE Select	ENSP00000356405.4:n.729+40_729+41insCA
ENST00000635846.1:c.729+40_729+41insCA	ENSP00000490035.1:n.729+40_729+41insCA
ENST00000643006.1:c.729+40_729+41insCA	ENSP00000496633.1:n.729+40_729+41insCA
ENST00000643784.1:c.*205+40_*205+41insCA	ENSP00000494944.1:n.*205+40_*205+41insCA
ENST00000647662.1:n.630+40_630+41insCA
ENST00000648071.1:c.*705+40_*705+41insCA	ENSP00000497513.1:n.*705+40_*705+41insCA
ENST00000649606.1:n.742+40_742+41insCA
ENST00000649895.1:n.947+40_947+41insCA
ENST00000650197.1:c.729+40_729+41insCA	ENSP00000496929.1:n.729+40_729+41insCA
ENST00000367435.3:c.729+40_729+41insCA	ENSP00000356405.3:n.729+40_729+41insCA
NM_024529.4:c.729+40_729+41insCA , LRG_507t1:c.729+40_729+41insCA	NP_078805.3:n.729+40_729+41insCA
XM_006711537.2:c.729+40_729+41insCA	XP_006711600.1:n.729+40_729+41insCA
XM_006711537.4:c.729+40_729+41insCA	XP_006711600.1:n.729+40_729+41insCA
NM_024529.5:c.729+40_729+41insCA MANE Select	NP_078805.3:n.729+40_729+41insCA