Canonical Allele Identifier: CA1028482256

Gene: NCOA1

Linked Data

• gnomAD v3: 2-24768516-C-CAAAAAAAAAAAAAAAAAAAAAAAAAAA
• gnomAD v4: 2-24768516-C-CAAAAAAAAAAAAAAAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768541_24768542insAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000664.2:g.24768541_24768542insAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000002.11:g.24991410_24991411insAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000664.1:g.24991410_24991411insAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000002.10:g.24844914_24844915insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_029014.1:g.189065_189066insAAAAAAAAAAAAAAAAAAAAAAAAAAA
NG_029014.2:g.281492_281493insAAAAAAAAAAAAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348332.8:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select	ENSP00000320940.5:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000288599.9:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000288599.5:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000348332.7:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000320940.5:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000395856.3:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000379197.3:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000405141.5:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000385097.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000406961.5:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000385216.1:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000407230.5:c.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000385195.1:n.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_003743.4:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_003734.3:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_147223.2:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_671756.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_147233.2:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_671766.1:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_005264625.1:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_005264682.1:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_005264626.1:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_005264683.1:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_005264627.1:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_005264684.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_005264628.1:c.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_005264685.1:n.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_011533141.1:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_011531443.1:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_001362950.1:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_001349879.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_001362952.1:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_001349881.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_001362954.1:c.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_001349883.1:n.*330_*331insAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_001362955.1:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_001349884.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_003743.5:c.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select	NP_003734.3:n.*150_*151insAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_147223.3:c.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_671756.1:n.*333_*334insAAAAAAAAAAAAAAAAAAAAAAAAAAA