Canonical Allele Identifier: CA376624980

Gene: NCOA4

Linked Data

• MyVariant Identifiers: chr10:g.51568366C>A (hg19) ; chr10:g.46027456G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027456G>T , CM000672.2:g.46027456G>T	GRCh38
NC_000010.10:g.51568366C>A , CM000672.1:g.51568366C>A	GRCh37
NC_000010.9:g.51238372C>A	NCBI36
NG_023372.1:g.8259C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000581486.6:c.-15+3070C>A MANE Select	ENSP00000462943.1:n.-15+3070C>A
ENST00000578454.5:c.10C>A	ENSP00000463027.1:p.Gln4Lys
ENST00000579039.2:c.10C>A	ENSP00000463455.1:p.Gln4Lys
ENST00000580070.5:c.-128+3070C>A	ENSP00000462352.1:n.-128+3070C>A
ENST00000581486.5:c.-15+3070C>A	ENSP00000462943.1:n.-15+3070C>A
ENST00000585056.5:c.-71+3070C>A	ENSP00000463022.1:n.-71+3070C>A
NM_001145260.1:c.10C>A	NP_001138732.1:p.Gln4Lys
NM_001145261.1:c.10C>A	NP_001138733.1:p.Gln4Lys
NM_001145263.1:c.-15+3070C>A	NP_001138735.1:n.-15+3070C>A
NM_001145260.2:c.10C>A	NP_001138732.1:p.Gln4Lys
NM_001145261.2:c.10C>A	NP_001138733.1:p.Gln4Lys
NM_001145263.2:c.-15+3070C>A MANE Select	NP_001138735.1:n.-15+3070C>A