Canonical Allele Identifier: CA43669199

Gene: NCOA1

Linked Data

• dbSNP Id: rs981208885
• gnomAD v3: 2-24751893-T-C
• gnomAD v4: 2-24751893-T-C
• MyVariant Identifiers: chr2:g.24974762T>C (hg19) ; chr2:g.24751893T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24751893T>C , CM000664.2:g.24751893T>C	GRCh38
NC_000002.11:g.24974762T>C , CM000664.1:g.24974762T>C	GRCh37
NC_000002.10:g.24828266T>C	NCBI36
NG_029014.1:g.172417T>C
NG_029014.2:g.264844T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348332.8:c.3707-89T>C MANE Select	ENSP00000320940.5:n.3707-89T>C
ENST00000288599.9:c.3707-89T>C	ENSP00000288599.5:n.3707-89T>C
ENST00000348332.7:c.3707-89T>C	ENSP00000320940.5:n.3707-89T>C
ENST00000395856.3:c.3707-89T>C	ENSP00000379197.3:n.3707-89T>C
ENST00000405141.5:c.3707-89T>C	ENSP00000385097.1:n.3707-89T>C
ENST00000406961.5:c.3707-89T>C	ENSP00000385216.1:n.3707-89T>C
ENST00000407230.5:c.3254-89T>C	ENSP00000385195.1:n.3254-89T>C
NM_003743.4:c.3707-89T>C	NP_003734.3:n.3707-89T>C
NM_147223.2:c.3707-89T>C	NP_671756.1:n.3707-89T>C
NM_147233.2:c.3707-89T>C	NP_671766.1:n.3707-89T>C
XM_005264625.1:c.3707-89T>C	XP_005264682.1:n.3707-89T>C
XM_005264626.1:c.3707-89T>C	XP_005264683.1:n.3707-89T>C
XM_005264627.1:c.3707-89T>C	XP_005264684.1:n.3707-89T>C
XM_005264628.1:c.3707-89T>C	XP_005264685.1:n.3707-89T>C
XM_011533141.1:c.3392-89T>C	XP_011531443.1:n.3392-89T>C
NM_001362950.1:c.3707-89T>C	NP_001349879.1:n.3707-89T>C
NM_001362952.1:c.3707-89T>C	NP_001349881.1:n.3707-89T>C
NM_001362954.1:c.3707-89T>C	NP_001349883.1:n.3707-89T>C
NM_001362955.1:c.3707-89T>C	NP_001349884.1:n.3707-89T>C
NM_003743.5:c.3707-89T>C MANE Select	NP_003734.3:n.3707-89T>C
NM_147223.3:c.3707-89T>C	NP_671756.1:n.3707-89T>C