Canonical Allele Identifier: CA1239046819

Gene: NCOA1

Linked Data

• dbSNP Id: rs1665186936

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768613_24768615del , CM000664.2:g.24768613_24768615del	GRCh38
NC_000002.11:g.24991482_24991484del , CM000664.1:g.24991482_24991484del	GRCh37
NC_000002.10:g.24844986_24844988del	NCBI36
NG_029014.1:g.189137_189139del
NG_029014.2:g.281564_281566del

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.*222_*224del MANE Select	ENSP00000320940.5:n.*222_*224del
ENST00000288599.9:c.*405_*407del	ENSP00000288599.5:n.*405_*407del
ENST00000348332.7:c.*222_*224del	ENSP00000320940.5:n.*222_*224del
ENST00000395856.3:c.*222_*224del	ENSP00000379197.3:n.*222_*224del
ENST00000405141.5:c.*405_*407del	ENSP00000385097.1:n.*405_*407del
ENST00000406961.5:c.*222_*224del	ENSP00000385216.1:n.*222_*224del
NM_003743.4:c.*222_*224del	NP_003734.3:n.*222_*224del
NM_147223.2:c.*405_*407del	NP_671756.1:n.*405_*407del
NM_147233.2:c.*222_*224del	NP_671766.1:n.*222_*224del
XM_005264625.1:c.*222_*224del	XP_005264682.1:n.*222_*224del
XM_005264626.1:c.*222_*224del	XP_005264683.1:n.*222_*224del
XM_005264627.1:c.*405_*407del	XP_005264684.1:n.*405_*407del
XM_005264628.1:c.*402_*404del	XP_005264685.1:n.*402_*404del
XM_011533141.1:c.*222_*224del	XP_011531443.1:n.*222_*224del
NM_001362950.1:c.*405_*407del	NP_001349879.1:n.*405_*407del
NM_001362952.1:c.*405_*407del	NP_001349881.1:n.*405_*407del
NM_001362954.1:c.*402_*404del	NP_001349883.1:n.*402_*404del
NM_001362955.1:c.*405_*407del	NP_001349884.1:n.*405_*407del
NM_003743.5:c.*222_*224del MANE Select	NP_003734.3:n.*222_*224del
NM_147223.3:c.*405_*407del	NP_671756.1:n.*405_*407del