Canonical Allele Identifier: CA2658131905

Gene: NCOA1

Linked Data

• gnomAD v4: 2-24768710-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768710G>C , CM000664.2:g.24768710G>C	GRCh38
NC_000002.11:g.24991579G>C , CM000664.1:g.24991579G>C	GRCh37
NC_000002.10:g.24845083G>C	NCBI36
NG_029014.1:g.189234G>C
NG_029014.2:g.281661G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.*319G>C MANE Select	ENSP00000320940.5:n.*319G>C
ENST00000288599.9:c.*502G>C	ENSP00000288599.5:n.*502G>C
ENST00000348332.7:c.*319G>C	ENSP00000320940.5:n.*319G>C
ENST00000395856.3:c.*319G>C	ENSP00000379197.3:n.*319G>C
ENST00000405141.5:c.*502G>C	ENSP00000385097.1:n.*502G>C
ENST00000406961.5:c.*319G>C	ENSP00000385216.1:n.*319G>C
NM_003743.4:c.*319G>C	NP_003734.3:n.*319G>C
NM_147223.2:c.*502G>C	NP_671756.1:n.*502G>C
NM_147233.2:c.*319G>C	NP_671766.1:n.*319G>C
XM_005264625.1:c.*319G>C	XP_005264682.1:n.*319G>C
XM_005264626.1:c.*319G>C	XP_005264683.1:n.*319G>C
XM_005264627.1:c.*502G>C	XP_005264684.1:n.*502G>C
XM_005264628.1:c.*499G>C	XP_005264685.1:n.*499G>C
XM_011533141.1:c.*319G>C	XP_011531443.1:n.*319G>C
NM_001362950.1:c.*502G>C	NP_001349879.1:n.*502G>C
NM_001362952.1:c.*502G>C	NP_001349881.1:n.*502G>C
NM_001362954.1:c.*499G>C	NP_001349883.1:n.*499G>C
NM_001362955.1:c.*502G>C	NP_001349884.1:n.*502G>C
NM_003743.5:c.*319G>C MANE Select	NP_003734.3:n.*319G>C
NM_147223.3:c.*502G>C	NP_671756.1:n.*502G>C