Canonical Allele Identifier: CA2658131728

Gene: NCOA1

Linked Data

• gnomAD v4: 2-24768493-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768493T>A , CM000664.2:g.24768493T>A	GRCh38
NC_000002.11:g.24991362T>A , CM000664.1:g.24991362T>A	GRCh37
NC_000002.10:g.24844866T>A	NCBI36
NG_029014.1:g.189017T>A
NG_029014.2:g.281444T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348332.8:c.*102T>A MANE Select	ENSP00000320940.5:n.*102T>A
ENST00000288599.9:c.*285T>A	ENSP00000288599.5:n.*285T>A
ENST00000348332.7:c.*102T>A	ENSP00000320940.5:n.*102T>A
ENST00000395856.3:c.*102T>A	ENSP00000379197.3:n.*102T>A
ENST00000405141.5:c.*285T>A	ENSP00000385097.1:n.*285T>A
ENST00000406961.5:c.*102T>A	ENSP00000385216.1:n.*102T>A
ENST00000407230.5:c.*282T>A	ENSP00000385195.1:n.*282T>A
NM_003743.4:c.*102T>A	NP_003734.3:n.*102T>A
NM_147223.2:c.*285T>A	NP_671756.1:n.*285T>A
NM_147233.2:c.*102T>A	NP_671766.1:n.*102T>A
XM_005264625.1:c.*102T>A	XP_005264682.1:n.*102T>A
XM_005264626.1:c.*102T>A	XP_005264683.1:n.*102T>A
XM_005264627.1:c.*285T>A	XP_005264684.1:n.*285T>A
XM_005264628.1:c.*282T>A	XP_005264685.1:n.*282T>A
XM_011533141.1:c.*102T>A	XP_011531443.1:n.*102T>A
NM_001362950.1:c.*285T>A	NP_001349879.1:n.*285T>A
NM_001362952.1:c.*285T>A	NP_001349881.1:n.*285T>A
NM_001362954.1:c.*282T>A	NP_001349883.1:n.*282T>A
NM_001362955.1:c.*285T>A	NP_001349884.1:n.*285T>A
NM_003743.5:c.*102T>A MANE Select	NP_003734.3:n.*102T>A
NM_147223.3:c.*285T>A	NP_671756.1:n.*285T>A