Canonical Allele Identifier: CA1239039635
Gene: NCOA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24751992C= , CM000664.2:g.24751992C= GRCh38
NC_000002.11:g.24974861C= , CM000664.1:g.24974861C= GRCh37
NC_000002.10:g.24828365C= NCBI36
NG_029014.1:g.172516C=
NG_029014.2:g.264943C=

Transcript Alleles

HGVS Amino-acid change
ENST00000348332.8:c.3717C= MANE Select ENSP00000320940.5:p.Pro1239=
ENST00000288599.9:c.3717C= ENSP00000288599.5:p.Pro1239=
ENST00000348332.7:c.3717C= ENSP00000320940.5:p.Pro1239=
ENST00000395856.3:c.3717C= ENSP00000379197.3:p.Pro1239=
ENST00000405141.5:c.3717C= ENSP00000385097.1:p.Pro1239=
ENST00000406961.5:c.3717C= ENSP00000385216.1:p.Pro1239=
ENST00000407230.5:c.3264C= ENSP00000385195.1:p.Pro1088=
NM_003743.4:c.3717C= NP_003734.3:p.Pro1239=
NM_147223.2:c.3717C= NP_671756.1:p.Pro1239=
NM_147233.2:c.3717C= NP_671766.1:p.Pro1239=
XM_005264625.1:c.3717C= XP_005264682.1:p.Pro1239=
XM_005264626.1:c.3717C= XP_005264683.1:p.Pro1239=
XM_005264627.1:c.3717C= XP_005264684.1:p.Pro1239=
XM_005264628.1:c.3717C= XP_005264685.1:p.Pro1239=
XM_011533141.1:c.3402C= XP_011531443.1:p.Pro1134=
NM_001362950.1:c.3717C= NP_001349879.1:p.Pro1239=
NM_001362952.1:c.3717C= NP_001349881.1:p.Pro1239=
NM_001362954.1:c.3717C= NP_001349883.1:p.Pro1239=
NM_001362955.1:c.3717C= NP_001349884.1:p.Pro1239=
NM_003743.5:c.3717C= MANE Select NP_003734.3:p.Pro1239=
NM_147223.3:c.3717C= NP_671756.1:p.Pro1239=