Canonical Allele Identifier: CA1552703
Gene: NCOA1 HGNC NCBI

Linked Data

dbSNP Id: rs764666047
gnomAD v2: 2-24974865-G-A
gnomAD v4: 2-24751996-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24751996G>A , CM000664.2:g.24751996G>A GRCh38
NC_000002.11:g.24974865G>A , CM000664.1:g.24974865G>A GRCh37
NC_000002.10:g.24828369G>A NCBI36
NG_029014.1:g.172520G>A
NG_029014.2:g.264947G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000348332.8:c.3721G>A MANE Select ENSP00000320940.5:p.Gly1241Ser
ENST00000288599.9:c.3721G>A ENSP00000288599.5:p.Gly1241Ser
ENST00000348332.7:c.3721G>A ENSP00000320940.5:p.Gly1241Ser
ENST00000395856.3:c.3721G>A ENSP00000379197.3:p.Gly1241Ser
ENST00000405141.5:c.3721G>A ENSP00000385097.1:p.Gly1241Ser
ENST00000406961.5:c.3721G>A ENSP00000385216.1:p.Gly1241Ser
ENST00000407230.5:c.3268G>A ENSP00000385195.1:p.Gly1090Ser
NM_003743.4:c.3721G>A NP_003734.3:p.Gly1241Ser
NM_147223.2:c.3721G>A NP_671756.1:p.Gly1241Ser
NM_147233.2:c.3721G>A NP_671766.1:p.Gly1241Ser
XM_005264625.1:c.3721G>A XP_005264682.1:p.Gly1241Ser
XM_005264626.1:c.3721G>A XP_005264683.1:p.Gly1241Ser
XM_005264627.1:c.3721G>A XP_005264684.1:p.Gly1241Ser
XM_005264628.1:c.3721G>A XP_005264685.1:p.Gly1241Ser
XM_011533141.1:c.3406G>A XP_011531443.1:p.Gly1136Ser
NM_001362950.1:c.3721G>A NP_001349879.1:p.Gly1241Ser
NM_001362952.1:c.3721G>A NP_001349881.1:p.Gly1241Ser
NM_001362954.1:c.3721G>A NP_001349883.1:p.Gly1241Ser
NM_001362955.1:c.3721G>A NP_001349884.1:p.Gly1241Ser
NM_003743.5:c.3721G>A MANE Select NP_003734.3:p.Gly1241Ser
NM_147223.3:c.3721G>A NP_671756.1:p.Gly1241Ser