Canonical Allele Identifier: CA1239046836
Gene: NCOA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24768649T= , CM000664.2:g.24768649T= GRCh38
NC_000002.11:g.24991518T= , CM000664.1:g.24991518T= GRCh37
NC_000002.10:g.24845022T= NCBI36
NG_029014.1:g.189173T=
NG_029014.2:g.281600T=

Transcript Alleles

HGVS Amino-acid change
ENST00000348332.8:c.*258T= MANE Select ENSP00000320940.5:n.*258T=
ENST00000288599.9:c.*441T= ENSP00000288599.5:n.*441T=
ENST00000348332.7:c.*258T= ENSP00000320940.5:n.*258T=
ENST00000395856.3:c.*258T= ENSP00000379197.3:n.*258T=
ENST00000405141.5:c.*441T= ENSP00000385097.1:n.*441T=
ENST00000406961.5:c.*258T= ENSP00000385216.1:n.*258T=
NM_003743.4:c.*258T= NP_003734.3:n.*258T=
NM_147223.2:c.*441T= NP_671756.1:n.*441T=
NM_147233.2:c.*258T= NP_671766.1:n.*258T=
XM_005264625.1:c.*258T= XP_005264682.1:n.*258T=
XM_005264626.1:c.*258T= XP_005264683.1:n.*258T=
XM_005264627.1:c.*441T= XP_005264684.1:n.*441T=
XM_005264628.1:c.*438T= XP_005264685.1:n.*438T=
XM_011533141.1:c.*258T= XP_011531443.1:n.*258T=
NM_001362950.1:c.*441T= NP_001349879.1:n.*441T=
NM_001362952.1:c.*441T= NP_001349881.1:n.*441T=
NM_001362954.1:c.*438T= NP_001349883.1:n.*438T=
NM_001362955.1:c.*441T= NP_001349884.1:n.*441T=
NM_003743.5:c.*258T= MANE Select NP_003734.3:n.*258T=
NM_147223.3:c.*441T= NP_671756.1:n.*441T=