Canonical Allele Identifier: CA1239046761
Gene: NCOA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24768515G= , CM000664.2:g.24768515G= GRCh38
NC_000002.11:g.24991384G= , CM000664.1:g.24991384G= GRCh37
NC_000002.10:g.24844888G= NCBI36
NG_029014.1:g.189039G=
NG_029014.2:g.281466G=

Transcript Alleles

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