Canonical Allele Identifier: CA2609004586

Gene: NCOA4

Linked Data

• gnomAD v4: 10-46027582-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027587del , CM000672.2:g.46027587del	GRCh38
NC_000010.10:g.51568239del , CM000672.1:g.51568239del	GRCh37
NC_000010.9:g.51238245del	NCBI36
NG_023372.1:g.8132del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581486.6:c.-15+2943del MANE Select	ENSP00000462943.1:n.-15+2943del
ENST00000578454.5:c.-63-55del	ENSP00000463027.1:n.-63-55del
ENST00000579039.2:c.-63-55del	ENSP00000463455.1:n.-63-55del
ENST00000580070.5:c.-128+2943del	ENSP00000462352.1:n.-128+2943del
ENST00000581486.5:c.-15+2943del	ENSP00000462943.1:n.-15+2943del
ENST00000585056.5:c.-71+2943del	ENSP00000463022.1:n.-71+2943del
NM_001145260.1:c.-63-55del	NP_001138732.1:n.-63-55del
NM_001145261.1:c.-63-55del	NP_001138733.1:n.-63-55del
NM_001145263.1:c.-15+2943del	NP_001138735.1:n.-15+2943del
NM_001145260.2:c.-63-55del	NP_001138732.1:n.-63-55del
NM_001145261.2:c.-63-55del	NP_001138733.1:n.-63-55del
NM_001145263.2:c.-15+2943del MANE Select	NP_001138735.1:n.-15+2943del