Canonical Allele Identifier: CA2658131854

Gene: NCOA1

Linked Data

• gnomAD v4: 2-24768676-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768676T>G , CM000664.2:g.24768676T>G	GRCh38
NC_000002.11:g.24991545T>G , CM000664.1:g.24991545T>G	GRCh37
NC_000002.10:g.24845049T>G	NCBI36
NG_029014.1:g.189200T>G
NG_029014.2:g.281627T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.*285T>G MANE Select	ENSP00000320940.5:n.*285T>G
ENST00000288599.9:c.*468T>G	ENSP00000288599.5:n.*468T>G
ENST00000348332.7:c.*285T>G	ENSP00000320940.5:n.*285T>G
ENST00000395856.3:c.*285T>G	ENSP00000379197.3:n.*285T>G
ENST00000405141.5:c.*468T>G	ENSP00000385097.1:n.*468T>G
ENST00000406961.5:c.*285T>G	ENSP00000385216.1:n.*285T>G
NM_003743.4:c.*285T>G	NP_003734.3:n.*285T>G
NM_147223.2:c.*468T>G	NP_671756.1:n.*468T>G
NM_147233.2:c.*285T>G	NP_671766.1:n.*285T>G
XM_005264625.1:c.*285T>G	XP_005264682.1:n.*285T>G
XM_005264626.1:c.*285T>G	XP_005264683.1:n.*285T>G
XM_005264627.1:c.*468T>G	XP_005264684.1:n.*468T>G
XM_005264628.1:c.*465T>G	XP_005264685.1:n.*465T>G
XM_011533141.1:c.*285T>G	XP_011531443.1:n.*285T>G
NM_001362950.1:c.*468T>G	NP_001349879.1:n.*468T>G
NM_001362952.1:c.*468T>G	NP_001349881.1:n.*468T>G
NM_001362954.1:c.*465T>G	NP_001349883.1:n.*465T>G
NM_001362955.1:c.*468T>G	NP_001349884.1:n.*468T>G
NM_003743.5:c.*285T>G MANE Select	NP_003734.3:n.*285T>G
NM_147223.3:c.*468T>G	NP_671756.1:n.*468T>G