Canonical Allele Identifier: CA1962424050

Gene: CCDC73 EIF3M

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32604465_32604467delinsATT , CM000673.2:g.32604465_32604467delinsATT	GRCh38
NC_000011.9:g.32626011_32626013delinsATT , CM000673.1:g.32626011_32626013delinsATT	GRCh37
NC_000011.8:g.32582587_32582589delinsATT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335185.10:c.3031-1447_3031-1445delinsAAT (CCDC73) MANE Select	ENSP00000335325.5:n.3031-1447_3031-1445delinsAAT
ENST00000531120.6:c.*2066_*2068delinsATT (EIF3M) MANE Select	ENSP00000436049.1:n.*2066_*2068delinsATT
ENST00000335185.9:c.3031-1447_3031-1445delinsAAT (CCDC73)	ENSP00000335325.5:n.3031-1447_3031-1445delinsAAT
ENST00000528333.1:c.138-1447_138-1445delinsAAT (CCDC73)
ENST00000531120.5:c.*2066_*2068delinsATT (EIF3M)	ENSP00000436049.1:n.*2066_*2068delinsATT
NM_001008391.3:c.3031-1447_3031-1445delinsAAT (CCDC73)	NP_001008392.2:n.3031-1447_3031-1445delinsAAT
XM_011519840.1:c.*2066_*2068delinsATT (EIF3M)	XP_011518142.1:n.*2066_*2068delinsATT
XM_011520139.1:c.2773-1447_2773-1445delinsAAT (CCDC73)	XP_011518441.1:n.2773-1447_2773-1445delinsAAT
NM_006360.6:c.*2066_*2068delinsATT (EIF3M) MANE Select	NP_006351.2:n.*2066_*2068delinsATT
NM_001307929.2:c.*2066_*2068delinsATT (EIF3M)	NP_001294858.1:n.*2066_*2068delinsATT
NM_001008391.4:c.3031-1447_3031-1445delinsAAT (CCDC73) MANE Select	NP_001008392.2:n.3031-1447_3031-1445delinsAAT