Canonical Allele Identifier: CA469551866

Gene: NCOA4

Linked Data

• MyVariant Identifiers: chr10:g.51568374C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027448G>C , CM000672.2:g.46027448G>C	GRCh38
NC_000010.10:g.51568374C>G , CM000672.1:g.51568374C>G	GRCh37
NC_000010.9:g.51238380C>G	NCBI36
NG_023372.1:g.8267C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000581486.6:c.-15+3078C>G MANE Select	ENSP00000462943.1:n.-15+3078C>G
ENST00000578454.5:c.18C>G	ENSP00000463027.1:p.Thr6=
ENST00000579039.2:c.18C>G	ENSP00000463455.1:p.Thr6=
ENST00000580070.5:c.-128+3078C>G	ENSP00000462352.1:n.-128+3078C>G
ENST00000581486.5:c.-15+3078C>G	ENSP00000462943.1:n.-15+3078C>G
ENST00000585056.5:c.-71+3078C>G	ENSP00000463022.1:n.-71+3078C>G
NM_001145260.1:c.18C>G	NP_001138732.1:p.Thr6=
NM_001145261.1:c.18C>G	NP_001138733.1:p.Thr6=
NM_001145263.1:c.-15+3078C>G	NP_001138735.1:n.-15+3078C>G
NM_001145260.2:c.18C>G	NP_001138732.1:p.Thr6=
NM_001145261.2:c.18C>G	NP_001138733.1:p.Thr6=
NM_001145263.2:c.-15+3078C>G MANE Select	NP_001138735.1:n.-15+3078C>G