Canonical Allele Identifier: CA2749192626

Gene: NCOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768526_24768541dup , CM000664.2:g.24768526_24768541dup	GRCh38
NC_000002.11:g.24991395_24991410dup , CM000664.1:g.24991395_24991410dup	GRCh37
NC_000002.10:g.24844899_24844914dup	NCBI36
NG_029014.1:g.189050_189065dup
NG_029014.2:g.281477_281492dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.*135_*150dup MANE Select	ENSP00000320940.5:n.*135_*150dup
ENST00000288599.9:c.*318_*333dup	ENSP00000288599.5:n.*318_*333dup
ENST00000348332.7:c.*135_*150dup	ENSP00000320940.5:n.*135_*150dup
ENST00000395856.3:c.*135_*150dup	ENSP00000379197.3:n.*135_*150dup
ENST00000405141.5:c.*318_*333dup	ENSP00000385097.1:n.*318_*333dup
ENST00000406961.5:c.*135_*150dup	ENSP00000385216.1:n.*135_*150dup
ENST00000407230.5:c.*315_*330dup	ENSP00000385195.1:n.*315_*330dup
NM_003743.4:c.*135_*150dup	NP_003734.3:n.*135_*150dup
NM_147223.2:c.*318_*333dup	NP_671756.1:n.*318_*333dup
NM_147233.2:c.*135_*150dup	NP_671766.1:n.*135_*150dup
XM_005264625.1:c.*135_*150dup	XP_005264682.1:n.*135_*150dup
XM_005264626.1:c.*135_*150dup	XP_005264683.1:n.*135_*150dup
XM_005264627.1:c.*318_*333dup	XP_005264684.1:n.*318_*333dup
XM_005264628.1:c.*315_*330dup	XP_005264685.1:n.*315_*330dup
XM_011533141.1:c.*135_*150dup	XP_011531443.1:n.*135_*150dup
NM_001362950.1:c.*318_*333dup	NP_001349879.1:n.*318_*333dup
NM_001362952.1:c.*318_*333dup	NP_001349881.1:n.*318_*333dup
NM_001362954.1:c.*315_*330dup	NP_001349883.1:n.*315_*330dup
NM_001362955.1:c.*318_*333dup	NP_001349884.1:n.*318_*333dup
NM_003743.5:c.*135_*150dup MANE Select	NP_003734.3:n.*135_*150dup
NM_147223.3:c.*318_*333dup	NP_671756.1:n.*318_*333dup