Canonical Allele Identifier: CA1028482253
Gene: NCOA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24768541_24768542insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000664.2:g.24768541_24768542insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000002.11:g.24991410_24991411insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000664.1:g.24991410_24991411insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000002.10:g.24844914_24844915insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_029014.1:g.189065_189066insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NG_029014.2:g.281492_281493insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000348332.8:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select ENSP00000320940.5:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000288599.9:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA ENSP00000288599.5:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000348332.7:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA ENSP00000320940.5:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000395856.3:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA ENSP00000379197.3:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000405141.5:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA ENSP00000385097.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000406961.5:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA ENSP00000385216.1:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000407230.5:c.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA ENSP00000385195.1:n.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA...
NM_003743.4:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NP_003734.3:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_147223.2:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NP_671756.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_147233.2:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NP_671766.1:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_005264625.1:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA XP_005264682.1:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_005264626.1:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA XP_005264683.1:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_005264627.1:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA XP_005264684.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_005264628.1:c.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA XP_005264685.1:n.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_011533141.1:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA XP_011531443.1:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_001362950.1:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NP_001349879.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_001362952.1:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NP_001349881.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_001362954.1:c.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NP_001349883.1:n.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_001362955.1:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NP_001349884.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_003743.5:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select NP_003734.3:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_147223.3:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NP_671756.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA