Canonical Allele Identifier: CA818533239

Gene: NCOA7 NCOA7-AS1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.125813790G>T , CM000668.2:g.125813790G>T	GRCh38
NC_000006.11:g.126134936G>T , CM000668.1:g.126134936G>T	GRCh37
NC_000006.10:g.126176629G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392477.7:c.-64-1501G>T (NCOA7) MANE Select	ENSP00000376269.2:n.-64-1501G>T
ENST00000229634.13:c.-155-1501G>T (NCOA7)	ENSP00000229634.9:n.-155-1501G>T
ENST00000368357.7:c.-64-1501G>T (NCOA7)	ENSP00000357341.3:n.-64-1501G>T
ENST00000392477.6:c.-64-1501G>T (NCOA7)	ENSP00000376269.2:n.-64-1501G>T
ENST00000417494.5:c.-64-1501G>T (NCOA7)	ENSP00000406363.1:n.-64-1501G>T
ENST00000428318.1:c.-64-1501G>T (NCOA7)	ENSP00000407426.1:n.-64-1501G>T
ENST00000453302.5:c.-64-1501G>T (NCOA7)	ENSP00000403643.1:n.-64-1501G>T
NM_001122842.2:c.-64-1501G>T (NCOA7)	NP_001116314.1:n.-64-1501G>T
NM_001199619.1:c.-64-1501G>T (NCOA7)	NP_001186548.1:n.-64-1501G>T
NM_001199620.1:c.-64-1501G>T (NCOA7)	NP_001186549.1:n.-64-1501G>T
NM_001199621.1:c.-155-1501G>T (NCOA7)	NP_001186550.1:n.-155-1501G>T
NM_181782.4:c.-64-1501G>T (NCOA7)	NP_861447.3:n.-64-1501G>T
NR_126386.1:n.49+5020C>A (NCOA7-AS1)
XM_005266822.3:c.-64-1501G>T (NCOA7)	XP_005266879.1:n.-64-1501G>T
XM_006715340.2:c.-64-1501G>T (NCOA7)	XP_006715403.1:n.-64-1501G>T
XM_011535455.1:c.-64-1501G>T (NCOA7)	XP_011533757.1:n.-64-1501G>T
XR_245505.1:n.306-1501G>T (NCOA7)
XM_005266822.4:c.-64-1501G>T (NCOA7)	XP_005266879.1:n.-64-1501G>T
XM_006715340.4:c.-64-1501G>T (NCOA7)	XP_006715403.1:n.-64-1501G>T
XM_011535455.2:c.-64-1501G>T (NCOA7)	XP_011533757.1:n.-64-1501G>T
XM_017010269.1:c.-64-1501G>T (NCOA7)	XP_016865758.1:n.-64-1501G>T
XM_017010270.1:c.-64-1501G>T (NCOA7)	XP_016865759.1:n.-64-1501G>T
XM_017010271.1:c.-64-1501G>T (NCOA7)	XP_016865760.1:n.-64-1501G>T
XM_017010272.2:c.-64-1501G>T (NCOA7)	XP_016865761.1:n.-64-1501G>T
XM_017010273.2:c.-64-1501G>T (NCOA7)	XP_016865762.1:n.-64-1501G>T
XM_017010274.2:c.-64-1501G>T (NCOA7)	XP_016865763.1:n.-64-1501G>T
XM_024446331.1:c.-64-1501G>T (NCOA7)	XP_024302099.1:n.-64-1501G>T
XM_024446332.1:c.-64-1501G>T (NCOA7)	XP_024302100.1:n.-64-1501G>T
XR_001743165.2:n.116-1501G>T (NCOA7)
NM_181782.5:c.-64-1501G>T (NCOA7) MANE Select	NP_861447.3:n.-64-1501G>T
NM_001122842.3:c.-64-1501G>T (NCOA7)	NP_001116314.1:n.-64-1501G>T
NM_001199619.2:c.-64-1501G>T (NCOA7)	NP_001186548.1:n.-64-1501G>T
NM_001199620.2:c.-64-1501G>T (NCOA7)	NP_001186549.1:n.-64-1501G>T
NM_001199621.2:c.-155-1501G>T (NCOA7)	NP_001186550.1:n.-155-1501G>T