Canonical Allele Identifier: CA1239046755
Gene: NCOA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24768506_24768507delinsGC , CM000664.2:g.24768506_24768507delinsGC GRCh38
NC_000002.11:g.24991375_24991376delinsGC , CM000664.1:g.24991375_24991376delinsGC GRCh37
NC_000002.10:g.24844879_24844880delinsGC NCBI36
NG_029014.1:g.189030_189031delinsGC
NG_029014.2:g.281457_281458delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000348332.8:c.*115_*116delinsGC MANE Select ENSP00000320940.5:n.*115_*116delinsGC
ENST00000288599.9:c.*298_*299delinsGC ENSP00000288599.5:n.*298_*299delinsGC
ENST00000348332.7:c.*115_*116delinsGC ENSP00000320940.5:n.*115_*116delinsGC
ENST00000395856.3:c.*115_*116delinsGC ENSP00000379197.3:n.*115_*116delinsGC
ENST00000405141.5:c.*298_*299delinsGC ENSP00000385097.1:n.*298_*299delinsGC
ENST00000406961.5:c.*115_*116delinsGC ENSP00000385216.1:n.*115_*116delinsGC
ENST00000407230.5:c.*295_*296delinsGC ENSP00000385195.1:n.*295_*296delinsGC
NM_003743.4:c.*115_*116delinsGC NP_003734.3:n.*115_*116delinsGC
NM_147223.2:c.*298_*299delinsGC NP_671756.1:n.*298_*299delinsGC
NM_147233.2:c.*115_*116delinsGC NP_671766.1:n.*115_*116delinsGC
XM_005264625.1:c.*115_*116delinsGC XP_005264682.1:n.*115_*116delinsGC
XM_005264626.1:c.*115_*116delinsGC XP_005264683.1:n.*115_*116delinsGC
XM_005264627.1:c.*298_*299delinsGC XP_005264684.1:n.*298_*299delinsGC
XM_005264628.1:c.*295_*296delinsGC XP_005264685.1:n.*295_*296delinsGC
XM_011533141.1:c.*115_*116delinsGC XP_011531443.1:n.*115_*116delinsGC
NM_001362950.1:c.*298_*299delinsGC NP_001349879.1:n.*298_*299delinsGC
NM_001362952.1:c.*298_*299delinsGC NP_001349881.1:n.*298_*299delinsGC
NM_001362954.1:c.*295_*296delinsGC NP_001349883.1:n.*295_*296delinsGC
NM_001362955.1:c.*298_*299delinsGC NP_001349884.1:n.*298_*299delinsGC
NM_003743.5:c.*115_*116delinsGC MANE Select NP_003734.3:n.*115_*116delinsGC
NM_147223.3:c.*298_*299delinsGC NP_671756.1:n.*298_*299delinsGC