Canonical Allele Identifier: CA2574556359

Gene: NCOA4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027405_46027415del , CM000672.2:g.46027405_46027415del	GRCh38
NC_000010.10:g.51568407_51568417del , CM000672.1:g.51568407_51568417del	GRCh37
NC_000010.9:g.51238413_51238423del	NCBI36
NG_023372.1:g.8300_8310del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581486.6:c.-15+3111_-15+3121del MANE Select	ENSP00000462943.1:n.-15+3111_-15+3121del
ENST00000578454.5:c.34+17_34+27del	ENSP00000463027.1:n.34+17_34+27del
ENST00000579039.2:c.34+17_34+27del	ENSP00000463455.1:n.34+17_34+27del
ENST00000580070.5:c.-128+3111_-128+3121del	ENSP00000462352.1:n.-128+3111_-128+3121del
ENST00000581486.5:c.-15+3111_-15+3121del	ENSP00000462943.1:n.-15+3111_-15+3121del
ENST00000585056.5:c.-71+3111_-71+3121del	ENSP00000463022.1:n.-71+3111_-71+3121del
NM_001145260.1:c.34+17_34+27del	NP_001138732.1:n.34+17_34+27del
NM_001145261.1:c.34+17_34+27del	NP_001138733.1:n.34+17_34+27del
NM_001145263.1:c.-15+3111_-15+3121del	NP_001138735.1:n.-15+3111_-15+3121del
NM_001145260.2:c.34+17_34+27del	NP_001138732.1:n.34+17_34+27del
NM_001145261.2:c.34+17_34+27del	NP_001138733.1:n.34+17_34+27del
NM_001145263.2:c.-15+3111_-15+3121del MANE Select	NP_001138735.1:n.-15+3111_-15+3121del