Canonical Allele Identifier: CA2712841027

Gene: NCOA7 NCOA7-AS1

Linked Data

• dbSNP Id: rs1775871514

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.125801358A>C , CM000668.2:g.125801358A>C	GRCh38
NC_000006.11:g.126122504A>C , CM000668.1:g.126122504A>C	GRCh37
NC_000006.10:g.126164197A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392477.7:c.-65+10291A>C (NCOA7) MANE Select	ENSP00000376269.2:n.-65+10291A>C
ENST00000229634.13:c.-156+10291A>C (NCOA7)	ENSP00000229634.9:n.-156+10291A>C
ENST00000368357.7:c.-64-13933A>C (NCOA7)	ENSP00000357341.3:n.-64-13933A>C
ENST00000392477.6:c.-65+10291A>C (NCOA7)	ENSP00000376269.2:n.-65+10291A>C
ENST00000417494.5:c.-65+10291A>C (NCOA7)	ENSP00000406363.1:n.-65+10291A>C
ENST00000453302.5:c.-65+4561A>C (NCOA7)	ENSP00000403643.1:n.-65+4561A>C
NM_001122842.2:c.-65+10291A>C (NCOA7)	NP_001116314.1:n.-65+10291A>C
NM_001199619.1:c.-64-13933A>C (NCOA7)	NP_001186548.1:n.-64-13933A>C
NM_001199620.1:c.-65+4561A>C (NCOA7)	NP_001186549.1:n.-65+4561A>C
NM_001199621.1:c.-156+10291A>C (NCOA7)	NP_001186550.1:n.-156+10291A>C
NM_181782.4:c.-65+10291A>C (NCOA7)	NP_861447.3:n.-65+10291A>C
NR_126386.1:n.191+945T>G (NCOA7-AS1)
XM_005266822.3:c.-65+10164A>C (NCOA7)	XP_005266879.1:n.-65+10164A>C
XM_006715340.2:c.-64-13933A>C (NCOA7)	XP_006715403.1:n.-64-13933A>C
XM_011535455.1:c.-65+10989A>C (NCOA7)	XP_011533757.1:n.-65+10989A>C
XR_245505.1:n.305+10291A>C (NCOA7)
XM_005266822.4:c.-65+10164A>C (NCOA7)	XP_005266879.1:n.-65+10164A>C
XM_006715340.4:c.-64-13933A>C (NCOA7)	XP_006715403.1:n.-64-13933A>C
XM_011535455.2:c.-65+10989A>C (NCOA7)	XP_011533757.1:n.-65+10989A>C
XM_017010270.1:c.-64-13933A>C (NCOA7)	XP_016865759.1:n.-64-13933A>C
XM_017010271.1:c.-65+10989A>C (NCOA7)	XP_016865760.1:n.-65+10989A>C
XM_017010272.2:c.-65+4561A>C (NCOA7)	XP_016865761.1:n.-65+4561A>C
XM_017010273.2:c.-65+10164A>C (NCOA7)	XP_016865762.1:n.-65+10164A>C
XM_017010274.2:c.-64-13933A>C (NCOA7)	XP_016865763.1:n.-64-13933A>C
XM_024446331.1:c.-65+4561A>C (NCOA7)	XP_024302099.1:n.-65+4561A>C
XM_024446332.1:c.-65+4561A>C (NCOA7)	XP_024302100.1:n.-65+4561A>C
XR_001743165.2:n.115+10291A>C (NCOA7)
NM_181782.5:c.-65+10291A>C (NCOA7) MANE Select	NP_861447.3:n.-65+10291A>C
NM_001122842.3:c.-65+10291A>C (NCOA7)	NP_001116314.1:n.-65+10291A>C
NM_001199619.2:c.-64-13933A>C (NCOA7)	NP_001186548.1:n.-64-13933A>C
NM_001199620.2:c.-65+4561A>C (NCOA7)	NP_001186549.1:n.-65+4561A>C
NM_001199621.2:c.-156+10291A>C (NCOA7)	NP_001186550.1:n.-156+10291A>C