Canonical Allele Identifier: CA767144044

Gene: NCOA1

Linked Data

• dbSNP Id: rs1425263599
• gnomAD v3: 2-24768641-C-CT
• gnomAD v4: 2-24768641-C-CT
• MyVariant Identifiers: chr2:g.24991510_24991511insT (hg19) ; chr2:g.24768641_24768642insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768642dup , CM000664.2:g.24768642dup	GRCh38
NC_000002.11:g.24991511dup , CM000664.1:g.24991511dup	GRCh37
NC_000002.10:g.24845015dup	NCBI36
NG_029014.1:g.189166dup
NG_029014.2:g.281593dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348332.8:c.*251dup MANE Select	ENSP00000320940.5:n.*251dup
ENST00000288599.9:c.*434dup	ENSP00000288599.5:n.*434dup
ENST00000348332.7:c.*251dup	ENSP00000320940.5:n.*251dup
ENST00000395856.3:c.*251dup	ENSP00000379197.3:n.*251dup
ENST00000405141.5:c.*434dup	ENSP00000385097.1:n.*434dup
ENST00000406961.5:c.*251dup	ENSP00000385216.1:n.*251dup
NM_003743.4:c.*251dup	NP_003734.3:n.*251dup
NM_147223.2:c.*434dup	NP_671756.1:n.*434dup
NM_147233.2:c.*251dup	NP_671766.1:n.*251dup
XM_005264625.1:c.*251dup	XP_005264682.1:n.*251dup
XM_005264626.1:c.*251dup	XP_005264683.1:n.*251dup
XM_005264627.1:c.*434dup	XP_005264684.1:n.*434dup
XM_005264628.1:c.*431dup	XP_005264685.1:n.*431dup
XM_011533141.1:c.*251dup	XP_011531443.1:n.*251dup
NM_001362950.1:c.*434dup	NP_001349879.1:n.*434dup
NM_001362952.1:c.*434dup	NP_001349881.1:n.*434dup
NM_001362954.1:c.*431dup	NP_001349883.1:n.*431dup
NM_001362955.1:c.*434dup	NP_001349884.1:n.*434dup
NM_003743.5:c.*251dup MANE Select	NP_003734.3:n.*251dup
NM_147223.3:c.*434dup	NP_671756.1:n.*434dup