Canonical Allele Identifier: CA15971009

Gene: NCOA5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46073481T>C , CM000682.2:g.46073481T>C	GRCh38
NC_000020.10:g.44702120T>C , CM000682.1:g.44702120T>C	GRCh37
NC_000020.9:g.44135527T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020967.3:c.39-2945A>G MANE Select	NP_066018.1:n.39-2945A>G
ENST00000290231.11:c.39-2945A>G MANE Select	ENSP00000290231.6:n.39-2945A>G
NM_001348148.1:c.-277-2945A>G	NP_001335077.1:n.-277-2945A>G
NM_001348148.2:c.-277-2945A>G	NP_001335077.1:n.-277-2945A>G
NM_001348149.1:c.39-2945A>G	NP_001335078.1:n.39-2945A>G
NM_001348149.2:c.39-2945A>G	NP_001335078.1:n.39-2945A>G
NM_001348150.1:c.-8-2945A>G	NP_001335079.1:n.-8-2945A>G
NM_001348150.2:c.-8-2945A>G	NP_001335079.1:n.-8-2945A>G
NM_001348151.1:c.-277-2945A>G	NP_001335080.1:n.-277-2945A>G
NM_001348151.2:c.-277-2945A>G	NP_001335080.1:n.-277-2945A>G
NM_020967.2:c.39-2945A>G	NP_066018.1:n.39-2945A>G
ENST00000290231.10:c.39-2945A>G	ENSP00000290231.6:n.39-2945A>G
ENST00000372291.3:c.-277-2945A>G	ENSP00000361365.3:n.-277-2945A>G
XM_005260474.2:c.-277-2945A>G	XP_005260531.1:n.-277-2945A>G
XM_011528951.1:c.39-2945A>G	XP_011527253.1:n.39-2945A>G