Canonical Allele Identifier: CA665615815

Gene: NCOA4

Linked Data

• dbSNP Id: rs1224421522
• MyVariant Identifiers: chr10:g.46027479_46027480insCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027480_46027481dup , CM000672.2:g.46027480_46027481dup	GRCh38
NC_000010.10:g.51568341_51568342dup , CM000672.1:g.51568341_51568342dup	GRCh37
NC_000010.9:g.51238347_51238348dup	NCBI36
NG_023372.1:g.8234_8235dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581486.6:c.-15+3045_-15+3046dup MANE Select	ENSP00000462943.1:n.-15+3045_-15+3046dup
ENST00000578454.5:c.-16_-15dup	ENSP00000463027.1:n.-16_-15dup
ENST00000579039.2:c.-16_-15dup	ENSP00000463455.1:n.-16_-15dup
ENST00000580070.5:c.-128+3045_-128+3046dup	ENSP00000462352.1:n.-128+3045_-128+3046dup
ENST00000581486.5:c.-15+3045_-15+3046dup	ENSP00000462943.1:n.-15+3045_-15+3046dup
ENST00000585056.5:c.-71+3045_-71+3046dup	ENSP00000463022.1:n.-71+3045_-71+3046dup
NM_001145260.1:c.-16_-15dup	NP_001138732.1:n.-16_-15dup
NM_001145261.1:c.-16_-15dup	NP_001138733.1:n.-16_-15dup
NM_001145263.1:c.-15+3045_-15+3046dup	NP_001138735.1:n.-15+3045_-15+3046dup
NM_001145260.2:c.-16_-15dup	NP_001138732.1:n.-16_-15dup
NM_001145261.2:c.-16_-15dup	NP_001138733.1:n.-16_-15dup
NM_001145263.2:c.-15+3045_-15+3046dup MANE Select	NP_001138735.1:n.-15+3045_-15+3046dup