Canonical Allele Identifier: CA1661510124

Gene: NCOA7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.125795807A= , CM000668.2:g.125795807A=	GRCh38
NC_000006.11:g.126116953A= , CM000668.1:g.126116953A=	GRCh37
NC_000006.10:g.126158646A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392477.7:c.-65+4740A= MANE Select	ENSP00000376269.2:n.-65+4740A=
ENST00000229634.13:c.-156+4740A=	ENSP00000229634.9:n.-156+4740A=
ENST00000368357.7:c.-65+9594A=	ENSP00000357341.3:n.-65+9594A=
ENST00000392477.6:c.-65+4740A=	ENSP00000376269.2:n.-65+4740A=
ENST00000417494.5:c.-65+4740A=	ENSP00000406363.1:n.-65+4740A=
ENST00000453302.5:c.-182-873A=	ENSP00000403643.1:n.-182-873A=
NM_001122842.2:c.-65+4740A=	NP_001116314.1:n.-65+4740A=
NM_001199619.1:c.-65+9594A=	NP_001186548.1:n.-65+9594A=
NM_001199620.1:c.-182-873A=	NP_001186549.1:n.-182-873A=
NM_001199621.1:c.-156+4740A=	NP_001186550.1:n.-156+4740A=
NM_181782.4:c.-65+4740A=	NP_861447.3:n.-65+4740A=
XM_005266822.3:c.-65+4613A=	XP_005266879.1:n.-65+4613A=
XM_006715340.2:c.-65+14436A=	XP_006715403.1:n.-65+14436A=
XM_011535455.1:c.-65+5438A=	XP_011533757.1:n.-65+5438A=
XR_245505.1:n.305+4740A=
XM_005266822.4:c.-65+4613A=	XP_005266879.1:n.-65+4613A=
XM_006715340.4:c.-65+14436A=	XP_006715403.1:n.-65+14436A=
XM_011535455.2:c.-65+5438A=	XP_011533757.1:n.-65+5438A=
XM_017010270.1:c.-65+9594A=	XP_016865759.1:n.-65+9594A=
XM_017010271.1:c.-65+5438A=	XP_016865760.1:n.-65+5438A=
XM_017010272.2:c.-182-873A=	XP_016865761.1:n.-182-873A=
XM_017010273.2:c.-65+4613A=	XP_016865762.1:n.-65+4613A=
XM_017010274.2:c.-65+14436A=	XP_016865763.1:n.-65+14436A=
XM_024446331.1:c.-182-873A=	XP_024302099.1:n.-182-873A=
XM_024446332.1:c.-182-873A=	XP_024302100.1:n.-182-873A=
XR_001743165.2:n.115+4740A=
NM_181782.5:c.-65+4740A= MANE Select	NP_861447.3:n.-65+4740A=
NM_001122842.3:c.-65+4740A=	NP_001116314.1:n.-65+4740A=
NM_001199619.2:c.-65+9594A=	NP_001186548.1:n.-65+9594A=
NM_001199620.2:c.-182-873A=	NP_001186549.1:n.-182-873A=
NM_001199621.2:c.-156+4740A=	NP_001186550.1:n.-156+4740A=