Canonical Allele Identifier: CA469551864

Gene: NCOA4

Linked Data

• MyVariant Identifiers: chr10:g.51568377T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027445A>G , CM000672.2:g.46027445A>G	GRCh38
NC_000010.10:g.51568377T>C , CM000672.1:g.51568377T>C	GRCh37
NC_000010.9:g.51238383T>C	NCBI36
NG_023372.1:g.8270T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000581486.6:c.-15+3081T>C MANE Select	ENSP00000462943.1:n.-15+3081T>C
ENST00000578454.5:c.21T>C	ENSP00000463027.1:p.Thr7=
ENST00000579039.2:c.21T>C	ENSP00000463455.1:p.Thr7=
ENST00000580070.5:c.-128+3081T>C	ENSP00000462352.1:n.-128+3081T>C
ENST00000581486.5:c.-15+3081T>C	ENSP00000462943.1:n.-15+3081T>C
ENST00000585056.5:c.-71+3081T>C	ENSP00000463022.1:n.-71+3081T>C
NM_001145260.1:c.21T>C	NP_001138732.1:p.Thr7=
NM_001145261.1:c.21T>C	NP_001138733.1:p.Thr7=
NM_001145263.1:c.-15+3081T>C	NP_001138735.1:n.-15+3081T>C
NM_001145260.2:c.21T>C	NP_001138732.1:p.Thr7=
NM_001145261.2:c.21T>C	NP_001138733.1:p.Thr7=
NM_001145263.2:c.-15+3081T>C MANE Select	NP_001138735.1:n.-15+3081T>C