Canonical Allele Identifier: CA918665394

Gene: NCOA4

Linked Data

• dbSNP Id: rs1590183662

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027444_46027445del , CM000672.2:g.46027444_46027445del	GRCh38
NC_000010.10:g.51568379_51568380del , CM000672.1:g.51568379_51568380del	GRCh37
NC_000010.9:g.51238385_51238386del	NCBI36
NG_023372.1:g.8272_8273del

Transcript Alleles

HGVS	Amino-acid change
ENST00000581486.6:c.-15+3083_-15+3084del MANE Select	ENSP00000462943.1:n.-15+3083_-15+3084del
ENST00000578454.5:c.23_24del	ENSP00000463027.1:p.Phe8CysfsTer21
ENST00000579039.2:c.23_24del	ENSP00000463455.1:p.Phe8CysfsTer21
ENST00000580070.5:c.-128+3083_-128+3084del	ENSP00000462352.1:n.-128+3083_-128+3084de...
ENST00000581486.5:c.-15+3083_-15+3084del	ENSP00000462943.1:n.-15+3083_-15+3084del
ENST00000585056.5:c.-71+3083_-71+3084del	ENSP00000463022.1:n.-71+3083_-71+3084del
NM_001145260.1:c.23_24del	NP_001138732.1:p.Phe8CysfsTer21
NM_001145261.1:c.23_24del	NP_001138733.1:p.Phe8CysfsTer21
NM_001145263.1:c.-15+3083_-15+3084del	NP_001138735.1:n.-15+3083_-15+3084del
NM_001145260.2:c.23_24del	NP_001138732.1:p.Phe8CysfsTer21
NM_001145261.2:c.23_24del	NP_001138733.1:p.Phe8CysfsTer21
NM_001145263.2:c.-15+3083_-15+3084del MANE Select	NP_001138735.1:n.-15+3083_-15+3084del