Canonical Allele Identifier: CA469551849

Gene: NCOA4

Linked Data

• dbSNP Id: rs75778204
• gnomAD v2: 10-51568554-G-T
• gnomAD v3: 10-46027268-C-A
• gnomAD v4: 10-46027268-C-A
• MyVariant Identifiers: chr10:g.51568554G>T (hg19) ; chr10:g.46027268C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027268C>A , CM000672.2:g.46027268C>A	GRCh38
NC_000010.10:g.51568554G>T , CM000672.1:g.51568554G>T	GRCh37
NC_000010.9:g.51238560G>T	NCBI36
NG_023372.1:g.8447G>T

Transcript Alleles

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