Canonical Allele Identifier: CA1907224597

Gene: NCOA4

Linked Data

• dbSNP Id: rs1840210599

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027267_46027268insAA , CM000672.2:g.46027267_46027268insAA	GRCh38
NC_000010.10:g.51568554_51568555insTT , CM000672.1:g.51568554_51568555insTT	GRCh37
NC_000010.9:g.51238560_51238561insTT	NCBI36
NG_023372.1:g.8447_8448insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581486.6:c.-15+3258_-15+3259insTT MANE Select	ENSP00000462943.1:n.-15+3258_-15+3259insTT
ENST00000578454.5:c.34+164_34+165insTT	ENSP00000463027.1:n.34+164_34+165insTT
ENST00000579039.2:c.34+164_34+165insTT	ENSP00000463455.1:n.34+164_34+165insTT
ENST00000580070.5:c.-128+3258_-128+3259insTT	ENSP00000462352.1:n.-128+3258_-128+3259insTT
ENST00000581486.5:c.-15+3258_-15+3259insTT	ENSP00000462943.1:n.-15+3258_-15+3259insTT
ENST00000585056.5:c.-71+3258_-71+3259insTT	ENSP00000463022.1:n.-71+3258_-71+3259insTT
NM_001145260.1:c.34+164_34+165insTT	NP_001138732.1:n.34+164_34+165insTT
NM_001145261.1:c.34+164_34+165insTT	NP_001138733.1:n.34+164_34+165insTT
NM_001145263.1:c.-15+3258_-15+3259insTT	NP_001138735.1:n.-15+3258_-15+3259insTT
NM_001145260.2:c.34+164_34+165insTT	NP_001138732.1:n.34+164_34+165insTT
NM_001145261.2:c.34+164_34+165insTT	NP_001138733.1:n.34+164_34+165insTT
NM_001145263.2:c.-15+3258_-15+3259insTT MANE Select	NP_001138735.1:n.-15+3258_-15+3259insTT