Canonical Allele Identifier: CA2658131821

Gene: NCOA1

Linked Data

• gnomAD v4: 2-24768609-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768615dup , CM000664.2:g.24768615dup	GRCh38
NC_000002.11:g.24991484dup , CM000664.1:g.24991484dup	GRCh37
NC_000002.10:g.24844988dup	NCBI36
NG_029014.1:g.189139dup
NG_029014.2:g.281566dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.*224dup MANE Select	ENSP00000320940.5:n.*224dup
ENST00000288599.9:c.*407dup	ENSP00000288599.5:n.*407dup
ENST00000348332.7:c.*224dup	ENSP00000320940.5:n.*224dup
ENST00000395856.3:c.*224dup	ENSP00000379197.3:n.*224dup
ENST00000405141.5:c.*407dup	ENSP00000385097.1:n.*407dup
ENST00000406961.5:c.*224dup	ENSP00000385216.1:n.*224dup
NM_003743.4:c.*224dup	NP_003734.3:n.*224dup
NM_147223.2:c.*407dup	NP_671756.1:n.*407dup
NM_147233.2:c.*224dup	NP_671766.1:n.*224dup
XM_005264625.1:c.*224dup	XP_005264682.1:n.*224dup
XM_005264626.1:c.*224dup	XP_005264683.1:n.*224dup
XM_005264627.1:c.*407dup	XP_005264684.1:n.*407dup
XM_005264628.1:c.*404dup	XP_005264685.1:n.*404dup
XM_011533141.1:c.*224dup	XP_011531443.1:n.*224dup
NM_001362950.1:c.*407dup	NP_001349879.1:n.*407dup
NM_001362952.1:c.*407dup	NP_001349881.1:n.*407dup
NM_001362954.1:c.*404dup	NP_001349883.1:n.*404dup
NM_001362955.1:c.*407dup	NP_001349884.1:n.*407dup
NM_003743.5:c.*224dup MANE Select	NP_003734.3:n.*224dup
NM_147223.3:c.*407dup	NP_671756.1:n.*407dup