Canonical Allele Identifier: CA12304861
Gene: NCOA7 HGNC NCBI
NCOA7-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs11967627

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.125801418A>G , CM000668.2:g.125801418A>G GRCh38
NC_000006.11:g.126122564A>G , CM000668.1:g.126122564A>G GRCh37
NC_000006.10:g.126164257A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392477.7:c.-65+10351A>G (NCOA7) MANE Select ENSP00000376269.2:n.-65+10351A>G
ENST00000229634.13:c.-156+10351A>G (NCOA7) ENSP00000229634.9:n.-156+10351A>G
ENST00000368357.7:c.-64-13873A>G (NCOA7) ENSP00000357341.3:n.-64-13873A>G
ENST00000392477.6:c.-65+10351A>G (NCOA7) ENSP00000376269.2:n.-65+10351A>G
ENST00000417494.5:c.-65+10351A>G (NCOA7) ENSP00000406363.1:n.-65+10351A>G
ENST00000453302.5:c.-65+4621A>G (NCOA7) ENSP00000403643.1:n.-65+4621A>G
NM_001122842.2:c.-65+10351A>G (NCOA7) NP_001116314.1:n.-65+10351A>G
NM_001199619.1:c.-64-13873A>G (NCOA7) NP_001186548.1:n.-64-13873A>G
NM_001199620.1:c.-65+4621A>G (NCOA7) NP_001186549.1:n.-65+4621A>G
NM_001199621.1:c.-156+10351A>G (NCOA7) NP_001186550.1:n.-156+10351A>G
NM_181782.4:c.-65+10351A>G (NCOA7) NP_861447.3:n.-65+10351A>G
NR_126386.1:n.191+885T>C (NCOA7-AS1)
XM_005266822.3:c.-65+10224A>G (NCOA7) XP_005266879.1:n.-65+10224A>G
XM_006715340.2:c.-64-13873A>G (NCOA7) XP_006715403.1:n.-64-13873A>G
XM_011535455.1:c.-65+11049A>G (NCOA7) XP_011533757.1:n.-65+11049A>G
XR_245505.1:n.305+10351A>G (NCOA7)
XM_005266822.4:c.-65+10224A>G (NCOA7) XP_005266879.1:n.-65+10224A>G
XM_006715340.4:c.-64-13873A>G (NCOA7) XP_006715403.1:n.-64-13873A>G
XM_011535455.2:c.-65+11049A>G (NCOA7) XP_011533757.1:n.-65+11049A>G
XM_017010270.1:c.-64-13873A>G (NCOA7) XP_016865759.1:n.-64-13873A>G
XM_017010271.1:c.-65+11049A>G (NCOA7) XP_016865760.1:n.-65+11049A>G
XM_017010272.2:c.-65+4621A>G (NCOA7) XP_016865761.1:n.-65+4621A>G
XM_017010273.2:c.-65+10224A>G (NCOA7) XP_016865762.1:n.-65+10224A>G
XM_017010274.2:c.-64-13873A>G (NCOA7) XP_016865763.1:n.-64-13873A>G
XM_024446331.1:c.-65+4621A>G (NCOA7) XP_024302099.1:n.-65+4621A>G
XM_024446332.1:c.-65+4621A>G (NCOA7) XP_024302100.1:n.-65+4621A>G
XR_001743165.2:n.115+10351A>G (NCOA7)
NM_181782.5:c.-65+10351A>G (NCOA7) MANE Select NP_861447.3:n.-65+10351A>G
NM_001122842.3:c.-65+10351A>G (NCOA7) NP_001116314.1:n.-65+10351A>G
NM_001199619.2:c.-64-13873A>G (NCOA7) NP_001186548.1:n.-64-13873A>G
NM_001199620.2:c.-65+4621A>G (NCOA7) NP_001186549.1:n.-65+4621A>G
NM_001199621.2:c.-156+10351A>G (NCOA7) NP_001186550.1:n.-156+10351A>G