Canonical Allele Identifier: CA2658131834

Gene: NCOA1

Linked Data

• gnomAD v4: 2-24768633-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768633T>C , CM000664.2:g.24768633T>C	GRCh38
NC_000002.11:g.24991502T>C , CM000664.1:g.24991502T>C	GRCh37
NC_000002.10:g.24845006T>C	NCBI36
NG_029014.1:g.189157T>C
NG_029014.2:g.281584T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.*242T>C MANE Select	ENSP00000320940.5:n.*242T>C
ENST00000288599.9:c.*425T>C	ENSP00000288599.5:n.*425T>C
ENST00000348332.7:c.*242T>C	ENSP00000320940.5:n.*242T>C
ENST00000395856.3:c.*242T>C	ENSP00000379197.3:n.*242T>C
ENST00000405141.5:c.*425T>C	ENSP00000385097.1:n.*425T>C
ENST00000406961.5:c.*242T>C	ENSP00000385216.1:n.*242T>C
NM_003743.4:c.*242T>C	NP_003734.3:n.*242T>C
NM_147223.2:c.*425T>C	NP_671756.1:n.*425T>C
NM_147233.2:c.*242T>C	NP_671766.1:n.*242T>C
XM_005264625.1:c.*242T>C	XP_005264682.1:n.*242T>C
XM_005264626.1:c.*242T>C	XP_005264683.1:n.*242T>C
XM_005264627.1:c.*425T>C	XP_005264684.1:n.*425T>C
XM_005264628.1:c.*422T>C	XP_005264685.1:n.*422T>C
XM_011533141.1:c.*242T>C	XP_011531443.1:n.*242T>C
NM_001362950.1:c.*425T>C	NP_001349879.1:n.*425T>C
NM_001362952.1:c.*425T>C	NP_001349881.1:n.*425T>C
NM_001362954.1:c.*422T>C	NP_001349883.1:n.*422T>C
NM_001362955.1:c.*425T>C	NP_001349884.1:n.*425T>C
NM_003743.5:c.*242T>C MANE Select	NP_003734.3:n.*242T>C
NM_147223.3:c.*425T>C	NP_671756.1:n.*425T>C