Canonical Allele Identifier: CA43628854

Gene: NCOA1

Linked Data

• dbSNP Id: rs1045576498
• gnomAD v3: 2-24768652-G-A
• gnomAD v4: 2-24768652-G-A
• MyVariant Identifiers: chr2:g.24991521G>A (hg19) ; chr2:g.24768652G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768652G>A , CM000664.2:g.24768652G>A	GRCh38
NC_000002.11:g.24991521G>A , CM000664.1:g.24991521G>A	GRCh37
NC_000002.10:g.24845025G>A	NCBI36
NG_029014.1:g.189176G>A
NG_029014.2:g.281603G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348332.8:c.*261G>A MANE Select	ENSP00000320940.5:n.*261G>A
ENST00000288599.9:c.*444G>A	ENSP00000288599.5:n.*444G>A
ENST00000348332.7:c.*261G>A	ENSP00000320940.5:n.*261G>A
ENST00000395856.3:c.*261G>A	ENSP00000379197.3:n.*261G>A
ENST00000405141.5:c.*444G>A	ENSP00000385097.1:n.*444G>A
ENST00000406961.5:c.*261G>A	ENSP00000385216.1:n.*261G>A
NM_003743.4:c.*261G>A	NP_003734.3:n.*261G>A
NM_147223.2:c.*444G>A	NP_671756.1:n.*444G>A
NM_147233.2:c.*261G>A	NP_671766.1:n.*261G>A
XM_005264625.1:c.*261G>A	XP_005264682.1:n.*261G>A
XM_005264626.1:c.*261G>A	XP_005264683.1:n.*261G>A
XM_005264627.1:c.*444G>A	XP_005264684.1:n.*444G>A
XM_005264628.1:c.*441G>A	XP_005264685.1:n.*441G>A
XM_011533141.1:c.*261G>A	XP_011531443.1:n.*261G>A
NM_001362950.1:c.*444G>A	NP_001349879.1:n.*444G>A
NM_001362952.1:c.*444G>A	NP_001349881.1:n.*444G>A
NM_001362954.1:c.*441G>A	NP_001349883.1:n.*441G>A
NM_001362955.1:c.*444G>A	NP_001349884.1:n.*444G>A
NM_003743.5:c.*261G>A MANE Select	NP_003734.3:n.*261G>A
NM_147223.3:c.*444G>A	NP_671756.1:n.*444G>A