Canonical Allele Identifier: CA767143999

Gene: NCOA1

Linked Data

• dbSNP Id: rs772970404
• gnomAD v3: 2-24768516-CAAAAA-C
• gnomAD v4: 2-24768516-CAAAAA-C
• MyVariant Identifiers: chr2:g.24991386_24991390del (hg19) ; chr2:g.24768517_24768521del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768537_24768541del , CM000664.2:g.24768537_24768541del	GRCh38
NC_000002.11:g.24991406_24991410del , CM000664.1:g.24991406_24991410del	GRCh37
NC_000002.10:g.24844910_24844914del	NCBI36
NG_029014.1:g.189061_189065del
NG_029014.2:g.281488_281492del

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.*146_*150del MANE Select	ENSP00000320940.5:n.*146_*150del
ENST00000288599.9:c.*329_*333del	ENSP00000288599.5:n.*329_*333del
ENST00000348332.7:c.*146_*150del	ENSP00000320940.5:n.*146_*150del
ENST00000395856.3:c.*146_*150del	ENSP00000379197.3:n.*146_*150del
ENST00000405141.5:c.*329_*333del	ENSP00000385097.1:n.*329_*333del
ENST00000406961.5:c.*146_*150del	ENSP00000385216.1:n.*146_*150del
ENST00000407230.5:c.*326_*330del	ENSP00000385195.1:n.*326_*330del
NM_003743.4:c.*146_*150del	NP_003734.3:n.*146_*150del
NM_147223.2:c.*329_*333del	NP_671756.1:n.*329_*333del
NM_147233.2:c.*146_*150del	NP_671766.1:n.*146_*150del
XM_005264625.1:c.*146_*150del	XP_005264682.1:n.*146_*150del
XM_005264626.1:c.*146_*150del	XP_005264683.1:n.*146_*150del
XM_005264627.1:c.*329_*333del	XP_005264684.1:n.*329_*333del
XM_005264628.1:c.*326_*330del	XP_005264685.1:n.*326_*330del
XM_011533141.1:c.*146_*150del	XP_011531443.1:n.*146_*150del
NM_001362950.1:c.*329_*333del	NP_001349879.1:n.*329_*333del
NM_001362952.1:c.*329_*333del	NP_001349881.1:n.*329_*333del
NM_001362954.1:c.*326_*330del	NP_001349883.1:n.*326_*330del
NM_001362955.1:c.*329_*333del	NP_001349884.1:n.*329_*333del
NM_003743.5:c.*146_*150del MANE Select	NP_003734.3:n.*146_*150del
NM_147223.3:c.*329_*333del	NP_671756.1:n.*329_*333del