Canonical Allele Identifier: CA593319469

Gene: NCOA4

Linked Data

• dbSNP Id: rs34282889
• gnomAD v2: 10-51568533-C-CTTTTTT
• gnomAD v3: 10-46027268-C-CAAAAAA
• gnomAD v4: 10-46027268-C-CAAAAAA
• MyVariant Identifiers: chr10:g.51568533_51568534insTTTTTT (hg19) ; chr10:g.46027268_46027269insAAAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027283_46027288dup , CM000672.2:g.46027283_46027288dup	GRCh38
NC_000010.10:g.51568548_51568553dup , CM000672.1:g.51568548_51568553dup	GRCh37
NC_000010.9:g.51238554_51238559dup	NCBI36
NG_023372.1:g.8441_8446dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000581486.6:c.-15+3252_-15+3257dup MANE Select	ENSP00000462943.1:n.-15+3252_-15+3257dup
ENST00000578454.5:c.34+158_34+163dup	ENSP00000463027.1:n.34+158_34+163dup
ENST00000579039.2:c.34+158_34+163dup	ENSP00000463455.1:n.34+158_34+163dup
ENST00000580070.5:c.-128+3252_-128+3257dup	ENSP00000462352.1:n.-128+3252_-128+3257dup
ENST00000581486.5:c.-15+3252_-15+3257dup	ENSP00000462943.1:n.-15+3252_-15+3257dup
ENST00000585056.5:c.-71+3252_-71+3257dup	ENSP00000463022.1:n.-71+3252_-71+3257dup
NM_001145260.1:c.34+158_34+163dup	NP_001138732.1:n.34+158_34+163dup
NM_001145261.1:c.34+158_34+163dup	NP_001138733.1:n.34+158_34+163dup
NM_001145263.1:c.-15+3252_-15+3257dup	NP_001138735.1:n.-15+3252_-15+3257dup
NM_001145260.2:c.34+158_34+163dup	NP_001138732.1:n.34+158_34+163dup
NM_001145261.2:c.34+158_34+163dup	NP_001138733.1:n.34+158_34+163dup
NM_001145263.2:c.-15+3252_-15+3257dup MANE Select	NP_001138735.1:n.-15+3252_-15+3257dup