Canonical Allele Identifier: CA1239046831
Gene: NCOA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24768640T= , CM000664.2:g.24768640T= GRCh38
NC_000002.11:g.24991509T= , CM000664.1:g.24991509T= GRCh37
NC_000002.10:g.24845013T= NCBI36
NG_029014.1:g.189164T=
NG_029014.2:g.281591T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348332.8:c.*249T= MANE Select ENSP00000320940.5:n.*249T=
ENST00000288599.9:c.*432T= ENSP00000288599.5:n.*432T=
ENST00000348332.7:c.*249T= ENSP00000320940.5:n.*249T=
ENST00000395856.3:c.*249T= ENSP00000379197.3:n.*249T=
ENST00000405141.5:c.*432T= ENSP00000385097.1:n.*432T=
ENST00000406961.5:c.*249T= ENSP00000385216.1:n.*249T=
NM_003743.4:c.*249T= NP_003734.3:n.*249T=
NM_147223.2:c.*432T= NP_671756.1:n.*432T=
NM_147233.2:c.*249T= NP_671766.1:n.*249T=
XM_005264625.1:c.*249T= XP_005264682.1:n.*249T=
XM_005264626.1:c.*249T= XP_005264683.1:n.*249T=
XM_005264627.1:c.*432T= XP_005264684.1:n.*432T=
XM_005264628.1:c.*429T= XP_005264685.1:n.*429T=
XM_011533141.1:c.*249T= XP_011531443.1:n.*249T=
NM_001362950.1:c.*432T= NP_001349879.1:n.*432T=
NM_001362952.1:c.*432T= NP_001349881.1:n.*432T=
NM_001362954.1:c.*429T= NP_001349883.1:n.*429T=
NM_001362955.1:c.*432T= NP_001349884.1:n.*432T=
NM_003743.5:c.*249T= MANE Select NP_003734.3:n.*249T=
NM_147223.3:c.*432T= NP_671756.1:n.*432T=