Canonical Allele Identifier: CA593319468

Gene: NCOA4

Linked Data

• gnomAD v2: 10-51568553-T-TTTG
• MyVariant Identifiers: chr10:g.51568554_51568555delinsTTGGA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027268_46027269insCAA , CM000672.2:g.46027268_46027269insCAA	GRCh38
NC_000010.10:g.51568553_51568554insTTG , CM000672.1:g.51568553_51568554insTTG	GRCh37
NC_000010.9:g.51238559_51238560insTTG	NCBI36
NG_023372.1:g.8446_8447insTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000581486.6:c.-15+3257_-15+3258insTTG MANE Select	ENSP00000462943.1:n.-15+3257_-15+3258insTTG
ENST00000578454.5:c.34+163_34+164insTTG	ENSP00000463027.1:n.34+163_34+164insTTG
ENST00000579039.2:c.34+163_34+164insTTG	ENSP00000463455.1:n.34+163_34+164insTTG
ENST00000580070.5:c.-128+3257_-128+3258insTTG	ENSP00000462352.1:n.-128+3257_-128+3258insTTG
ENST00000581486.5:c.-15+3257_-15+3258insTTG	ENSP00000462943.1:n.-15+3257_-15+3258insTTG
ENST00000585056.5:c.-71+3257_-71+3258insTTG	ENSP00000463022.1:n.-71+3257_-71+3258insTTG
NM_001145260.1:c.34+163_34+164insTTG	NP_001138732.1:n.34+163_34+164insTTG
NM_001145261.1:c.34+163_34+164insTTG	NP_001138733.1:n.34+163_34+164insTTG
NM_001145263.1:c.-15+3257_-15+3258insTTG	NP_001138735.1:n.-15+3257_-15+3258insTTG
NM_001145260.2:c.34+163_34+164insTTG	NP_001138732.1:n.34+163_34+164insTTG
NM_001145261.2:c.34+163_34+164insTTG	NP_001138733.1:n.34+163_34+164insTTG
NM_001145263.2:c.-15+3257_-15+3258insTTG MANE Select	NP_001138735.1:n.-15+3257_-15+3258insTTG