Canonical Allele Identifier: CA43628648

Gene: NCOA1

Linked Data

• dbSNP Id: rs1491566461
• gnomAD v3: 2-24768515-GCA-G
• gnomAD v4: 2-24768515-GCA-G
• MyVariant Identifiers: chr2:g.24991385_24991386del (hg19) ; chr2:g.24768516_24768517del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768516_24768517del , CM000664.2:g.24768516_24768517del	GRCh38
NC_000002.11:g.24991385_24991386del , CM000664.1:g.24991385_24991386del	GRCh37
NC_000002.10:g.24844889_24844890del	NCBI36
NG_029014.1:g.189040_189041del
NG_029014.2:g.281467_281468del

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.*125_*126del MANE Select	ENSP00000320940.5:n.*125_*126del
ENST00000288599.9:c.*308_*309del	ENSP00000288599.5:n.*308_*309del
ENST00000348332.7:c.*125_*126del	ENSP00000320940.5:n.*125_*126del
ENST00000395856.3:c.*125_*126del	ENSP00000379197.3:n.*125_*126del
ENST00000405141.5:c.*308_*309del	ENSP00000385097.1:n.*308_*309del
ENST00000406961.5:c.*125_*126del	ENSP00000385216.1:n.*125_*126del
ENST00000407230.5:c.*305_*306del	ENSP00000385195.1:n.*305_*306del
NM_003743.4:c.*125_*126del	NP_003734.3:n.*125_*126del
NM_147223.2:c.*308_*309del	NP_671756.1:n.*308_*309del
NM_147233.2:c.*125_*126del	NP_671766.1:n.*125_*126del
XM_005264625.1:c.*125_*126del	XP_005264682.1:n.*125_*126del
XM_005264626.1:c.*125_*126del	XP_005264683.1:n.*125_*126del
XM_005264627.1:c.*308_*309del	XP_005264684.1:n.*308_*309del
XM_005264628.1:c.*305_*306del	XP_005264685.1:n.*305_*306del
XM_011533141.1:c.*125_*126del	XP_011531443.1:n.*125_*126del
NM_001362950.1:c.*308_*309del	NP_001349879.1:n.*308_*309del
NM_001362952.1:c.*308_*309del	NP_001349881.1:n.*308_*309del
NM_001362954.1:c.*305_*306del	NP_001349883.1:n.*305_*306del
NM_001362955.1:c.*308_*309del	NP_001349884.1:n.*308_*309del
NM_003743.5:c.*125_*126del MANE Select	NP_003734.3:n.*125_*126del
NM_147223.3:c.*308_*309del	NP_671756.1:n.*308_*309del