Canonical Allele Identifier: CA2367218964

Gene: NCOA3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.47639749A= , CM000682.2:g.47639749A=	GRCh38
NC_000020.10:g.46268493A= , CM000682.1:g.46268493A=	GRCh37
NC_000020.9:g.45701900A=	NCBI36
NG_016810.1:g.142893A=

Transcript Alleles

HGVS	Amino-acid Change
NM_181659.3:c.2880A= MANE Select	NP_858045.1:p.Thr960=
ENST00000371998.8:c.2880A= MANE Select	ENSP00000361066.3:p.Thr960=
NM_001174087.1:c.2880A=	NP_001167558.1:p.Thr960=
NM_001174087.2:c.2880A=	NP_001167558.1:p.Thr960=
NM_001174088.1:c.2865A=	NP_001167559.1:p.Thr955=
NM_001174088.2:c.2865A=	NP_001167559.1:p.Thr955=
NM_006534.3:c.2880A=	NP_006525.2:p.Thr960=
NM_006534.4:c.2880A=	NP_006525.2:p.Thr960=
NM_181659.2:c.2880A=	NP_858045.1:p.Thr960=
ENST00000371997.3:c.2865A=	ENSP00000361065.3:p.Thr955=
ENST00000371998.7:c.2880A=	ENSP00000361066.3:p.Thr960=
ENST00000372004.7:c.2880A=	ENSP00000361073.1:p.Thr960=