Canonical Allele Identifier: CA11147716
Gene: NCOA1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17737058

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24768700C>G , CM000664.2:g.24768700C>G GRCh38
NC_000002.10:g.24845073C>G NCBI36
NC_000002.11:g.24991569C>G , CM000664.1:g.24991569C>G GRCh37
NG_029014.1:g.189224C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000288599.9:c.*492C>G ENSP00000288599.5:p.=
ENST00000348332.7:c.*309C>G ENSP00000320940.5:p.=
ENST00000395856.3:c.*309C>G ENSP00000379197.3:p.=
ENST00000405141.5:c.*492C>G ENSP00000385097.1:p.=
ENST00000406961.5:c.*309C>G ENSP00000385216.1:p.=
NM_003743.4:c.*309C>G NP_003734.3:p.=
NM_147223.2:c.*492C>G NP_671756.1:p.=
NM_147233.2:c.*309C>G NP_671766.1:p.=
XM_005264625.1:c.*309C>G XP_005264682.1:p.=
XM_005264626.1:c.*309C>G XP_005264683.1:p.=
XM_005264627.1:c.*492C>G XP_005264684.1:p.=
XM_005264628.1:c.*489C>G XP_005264685.1:p.=
XM_011533141.1:c.*309C>G XP_011531443.1:p.=