Canonical Allele Identifier: CA43628655

Gene: NCOA1

Linked Data

• dbSNP Id: rs772970404
• gnomAD v3: 2-24768516-C-CAA
• gnomAD v4: 2-24768516-C-CAA
• MyVariant Identifiers: chr2:g.24991385_24991386insAA (hg19) ; chr2:g.24768516_24768517insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768540_24768541dup , CM000664.2:g.24768540_24768541dup	GRCh38
NC_000002.11:g.24991409_24991410dup , CM000664.1:g.24991409_24991410dup	GRCh37
NC_000002.10:g.24844913_24844914dup	NCBI36
NG_029014.1:g.189064_189065dup
NG_029014.2:g.281491_281492dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.*149_*150dup MANE Select	ENSP00000320940.5:n.*149_*150dup
ENST00000288599.9:c.*332_*333dup	ENSP00000288599.5:n.*332_*333dup
ENST00000348332.7:c.*149_*150dup	ENSP00000320940.5:n.*149_*150dup
ENST00000395856.3:c.*149_*150dup	ENSP00000379197.3:n.*149_*150dup
ENST00000405141.5:c.*332_*333dup	ENSP00000385097.1:n.*332_*333dup
ENST00000406961.5:c.*149_*150dup	ENSP00000385216.1:n.*149_*150dup
ENST00000407230.5:c.*329_*330dup	ENSP00000385195.1:n.*329_*330dup
NM_003743.4:c.*149_*150dup	NP_003734.3:n.*149_*150dup
NM_147223.2:c.*332_*333dup	NP_671756.1:n.*332_*333dup
NM_147233.2:c.*149_*150dup	NP_671766.1:n.*149_*150dup
XM_005264625.1:c.*149_*150dup	XP_005264682.1:n.*149_*150dup
XM_005264626.1:c.*149_*150dup	XP_005264683.1:n.*149_*150dup
XM_005264627.1:c.*332_*333dup	XP_005264684.1:n.*332_*333dup
XM_005264628.1:c.*329_*330dup	XP_005264685.1:n.*329_*330dup
XM_011533141.1:c.*149_*150dup	XP_011531443.1:n.*149_*150dup
NM_001362950.1:c.*332_*333dup	NP_001349879.1:n.*332_*333dup
NM_001362952.1:c.*332_*333dup	NP_001349881.1:n.*332_*333dup
NM_001362954.1:c.*329_*330dup	NP_001349883.1:n.*329_*330dup
NM_001362955.1:c.*332_*333dup	NP_001349884.1:n.*332_*333dup
NM_003743.5:c.*149_*150dup MANE Select	NP_003734.3:n.*149_*150dup
NM_147223.3:c.*332_*333dup	NP_671756.1:n.*332_*333dup