Canonical Allele Identifier: CA3987382
Gene: NCOA7 HGNC NCBI

Linked Data

dbSNP Id: rs1567

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.125928768T>G , CM000668.2:g.125928768T>G GRCh38
NC_000006.11:g.126249914T>G , CM000668.1:g.126249914T>G GRCh37
NC_000006.10:g.126291607T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392477.7:c.2826T>G MANE Select ENSP00000376269.2:p.Asp942Glu
ENST00000229634.13:c.2481T>G ENSP00000229634.9:p.Asp827Glu
ENST00000368357.7:c.2826T>G ENSP00000357341.3:p.Asp942Glu
ENST00000392477.6:c.2826T>G ENSP00000376269.2:p.Asp942Glu
ENST00000438495.6:c.657T>G ENSP00000398268.2:p.Asp219Glu
ENST00000444128.2:c.*103T>G ENSP00000407684.2:n.*103T>G
NM_001122842.2:c.2793T>G NP_001116314.1:p.Asp931Glu
NM_001199619.1:c.2826T>G NP_001186548.1:p.Asp942Glu
NM_001199620.1:c.2826T>G NP_001186549.1:p.Asp942Glu
NM_001199621.1:c.2481T>G NP_001186550.1:p.Asp827Glu
NM_001199622.1:c.657T>G NP_001186551.1:p.Asp219Glu
NM_181782.4:c.2826T>G NP_861447.3:p.Asp942Glu
XM_005266822.3:c.2826T>G XP_005266879.1:p.Asp942Glu
XM_006715340.2:c.2826T>G XP_006715403.1:p.Asp942Glu
XM_011535455.1:c.2826T>G XP_011533757.1:p.Asp942Glu
XM_005266822.4:c.2826T>G XP_005266879.1:p.Asp942Glu
XM_006715340.4:c.2826T>G XP_006715403.1:p.Asp942Glu
XM_011535455.2:c.2826T>G XP_011533757.1:p.Asp942Glu
XM_017010269.1:c.2826T>G XP_016865758.1:p.Asp942Glu
XM_017010270.1:c.2793T>G XP_016865759.1:p.Asp931Glu
XM_017010271.1:c.2793T>G XP_016865760.1:p.Asp931Glu
XM_017010272.2:c.2793T>G XP_016865761.1:p.Asp931Glu
XM_017010273.2:c.2793T>G XP_016865762.1:p.Asp931Glu
XM_017010274.2:c.2793T>G XP_016865763.1:p.Asp931Glu
XM_024446331.1:c.2826T>G XP_024302099.1:p.Asp942Glu
XM_024446332.1:c.2793T>G XP_024302100.1:p.Asp931Glu
XR_001743165.2:n.3073T>G
NM_181782.5:c.2826T>G MANE Select NP_861447.3:p.Asp942Glu
NM_001122842.3:c.2793T>G NP_001116314.1:p.Asp931Glu
NM_001199619.2:c.2826T>G NP_001186548.1:p.Asp942Glu
NM_001199620.2:c.2826T>G NP_001186549.1:p.Asp942Glu
NM_001199621.2:c.2481T>G NP_001186550.1:p.Asp827Glu
NM_001199622.2:c.657T>G NP_001186551.1:p.Asp219Glu