Canonical Allele Identifier: CA2838213016

Gene: NCOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24751938A>G , CM000664.2:g.24751938A>G	GRCh38
NC_000002.11:g.24974807A>G , CM000664.1:g.24974807A>G	GRCh37
NC_000002.10:g.24828311A>G	NCBI36
NG_029014.1:g.172462A>G
NG_029014.2:g.264889A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348332.8:c.3707-44A>G MANE Select	ENSP00000320940.5:n.3707-44A>G
ENST00000288599.9:c.3707-44A>G	ENSP00000288599.5:n.3707-44A>G
ENST00000348332.7:c.3707-44A>G	ENSP00000320940.5:n.3707-44A>G
ENST00000395856.3:c.3707-44A>G	ENSP00000379197.3:n.3707-44A>G
ENST00000405141.5:c.3707-44A>G	ENSP00000385097.1:n.3707-44A>G
ENST00000406961.5:c.3707-44A>G	ENSP00000385216.1:n.3707-44A>G
ENST00000407230.5:c.3254-44A>G	ENSP00000385195.1:n.3254-44A>G
NM_003743.4:c.3707-44A>G	NP_003734.3:n.3707-44A>G
NM_147223.2:c.3707-44A>G	NP_671756.1:n.3707-44A>G
NM_147233.2:c.3707-44A>G	NP_671766.1:n.3707-44A>G
XM_005264625.1:c.3707-44A>G	XP_005264682.1:n.3707-44A>G
XM_005264626.1:c.3707-44A>G	XP_005264683.1:n.3707-44A>G
XM_005264627.1:c.3707-44A>G	XP_005264684.1:n.3707-44A>G
XM_005264628.1:c.3707-44A>G	XP_005264685.1:n.3707-44A>G
XM_011533141.1:c.3392-44A>G	XP_011531443.1:n.3392-44A>G
NM_001362950.1:c.3707-44A>G	NP_001349879.1:n.3707-44A>G
NM_001362952.1:c.3707-44A>G	NP_001349881.1:n.3707-44A>G
NM_001362954.1:c.3707-44A>G	NP_001349883.1:n.3707-44A>G
NM_001362955.1:c.3707-44A>G	NP_001349884.1:n.3707-44A>G
NM_003743.5:c.3707-44A>G MANE Select	NP_003734.3:n.3707-44A>G
NM_147223.3:c.3707-44A>G	NP_671756.1:n.3707-44A>G