Canonical Allele Identifier: CA1239046814

Gene: NCOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768597G= , CM000664.2:g.24768597G=	GRCh38
NC_000002.11:g.24991466G= , CM000664.1:g.24991466G=	GRCh37
NC_000002.10:g.24844970G=	NCBI36
NG_029014.1:g.189121G=
NG_029014.2:g.281548G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348332.8:c.*206G= MANE Select	ENSP00000320940.5:n.*206G=
ENST00000288599.9:c.*389G=	ENSP00000288599.5:n.*389G=
ENST00000348332.7:c.*206G=	ENSP00000320940.5:n.*206G=
ENST00000395856.3:c.*206G=	ENSP00000379197.3:n.*206G=
ENST00000405141.5:c.*389G=	ENSP00000385097.1:n.*389G=
ENST00000406961.5:c.*206G=	ENSP00000385216.1:n.*206G=
NM_003743.4:c.*206G=	NP_003734.3:n.*206G=
NM_147223.2:c.*389G=	NP_671756.1:n.*389G=
NM_147233.2:c.*206G=	NP_671766.1:n.*206G=
XM_005264625.1:c.*206G=	XP_005264682.1:n.*206G=
XM_005264626.1:c.*206G=	XP_005264683.1:n.*206G=
XM_005264627.1:c.*389G=	XP_005264684.1:n.*389G=
XM_005264628.1:c.*386G=	XP_005264685.1:n.*386G=
XM_011533141.1:c.*206G=	XP_011531443.1:n.*206G=
NM_001362950.1:c.*389G=	NP_001349879.1:n.*389G=
NM_001362952.1:c.*389G=	NP_001349881.1:n.*389G=
NM_001362954.1:c.*386G=	NP_001349883.1:n.*386G=
NM_001362955.1:c.*389G=	NP_001349884.1:n.*389G=
NM_003743.5:c.*206G= MANE Select	NP_003734.3:n.*206G=
NM_147223.3:c.*389G=	NP_671756.1:n.*389G=