Canonical Allele Identifier: CA2658131748
Gene: NCOA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24768515_24768521del , CM000664.2:g.24768515_24768521del GRCh38
NC_000002.11:g.24991384_24991390del , CM000664.1:g.24991384_24991390del GRCh37
NC_000002.10:g.24844888_24844894del NCBI36
NG_029014.1:g.189039_189045del
NG_029014.2:g.281466_281472del

Transcript Alleles

HGVS Amino-acid Change
ENST00000348332.8:c.*124_*130del MANE Select ENSP00000320940.5:n.*124_*130del
ENST00000288599.9:c.*307_*313del ENSP00000288599.5:n.*307_*313del
ENST00000348332.7:c.*124_*130del ENSP00000320940.5:n.*124_*130del
ENST00000395856.3:c.*124_*130del ENSP00000379197.3:n.*124_*130del
ENST00000405141.5:c.*307_*313del ENSP00000385097.1:n.*307_*313del
ENST00000406961.5:c.*124_*130del ENSP00000385216.1:n.*124_*130del
ENST00000407230.5:c.*304_*310del ENSP00000385195.1:n.*304_*310del
NM_003743.4:c.*124_*130del NP_003734.3:n.*124_*130del
NM_147223.2:c.*307_*313del NP_671756.1:n.*307_*313del
NM_147233.2:c.*124_*130del NP_671766.1:n.*124_*130del
XM_005264625.1:c.*124_*130del XP_005264682.1:n.*124_*130del
XM_005264626.1:c.*124_*130del XP_005264683.1:n.*124_*130del
XM_005264627.1:c.*307_*313del XP_005264684.1:n.*307_*313del
XM_005264628.1:c.*304_*310del XP_005264685.1:n.*304_*310del
XM_011533141.1:c.*124_*130del XP_011531443.1:n.*124_*130del
NM_001362950.1:c.*307_*313del NP_001349879.1:n.*307_*313del
NM_001362952.1:c.*307_*313del NP_001349881.1:n.*307_*313del
NM_001362954.1:c.*304_*310del NP_001349883.1:n.*304_*310del
NM_001362955.1:c.*307_*313del NP_001349884.1:n.*307_*313del
NM_003743.5:c.*124_*130del MANE Select NP_003734.3:n.*124_*130del
NM_147223.3:c.*307_*313del NP_671756.1:n.*307_*313del