Canonical Allele Identifier: CA1344876385
Gene: BRPF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9745039C= , CM000665.2:g.9745039C= GRCh38
NC_000003.11:g.9786723C= , CM000665.1:g.9786723C= GRCh37
NC_000003.10:g.9761723C= NCBI36
NG_012106.1:g.96C=
NG_052955.1:g.18311C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000424362.7:c.2949C= ENSP00000398863.2:p.Asn983=
ENST00000457855.2:c.2931C= ENSP00000410210.2:p.Asn977=
ENST00000497565.3:n.1571C=
ENST00000672126.2:c.*566C= ENSP00000500718.1:n.*566C=
ENST00000672515.2:c.2949C= ENSP00000499951.2:p.Asn983=
ENST00000673551.2:c.*1075C= ENSP00000500672.1:n.*1075C=
ENST00000682208.1:c.2931C= ENSP00000508123.1:p.Asn977=
ENST00000682980.1:c.2664C= ENSP00000508198.1:p.Asn888=
ENST00000683423.1:c.*439C= ENSP00000507659.1:n.*439C=
ENST00000683639.1:c.2934C= ENSP00000506903.1:p.Asn978=
ENST00000683743.1:c.2934C= ENSP00000507469.1:p.Asn978=
ENST00000684199.1:c.2952C= ENSP00000506921.1:p.Asn984=
ENST00000684206.1:c.2646C= ENSP00000507148.1:p.Asn882=
ENST00000684333.1:c.2931C= ENSP00000508256.1:p.Asn977=
ENST00000684573.1:c.671C=
ENST00000684608.1:c.*1078C= ENSP00000507969.1:n.*1078C=
ENST00000383829.7:c.2952C= MANE Select ENSP00000373340.2:p.Asn984=
ENST00000424362.6:c.2931C= ENSP00000398863.1:p.Asn977=
ENST00000497565.2:n.1571C=
ENST00000672126.1:c.2867C= ENSP00000500718.1:n.2867C=
ENST00000672515.1:c.2926C=
ENST00000673551.1:c.*1075C= ENSP00000500672.1:n.*1075C=
ENST00000383829.6:c.2952C= ENSP00000373340.2:p.Asn984=
ENST00000424362.5:c.2931C= ENSP00000398863.1:p.Asn977=
ENST00000433861.6:c.2649C= ENSP00000402485.2:p.Asn883=
ENST00000457855.1:c.2934C= ENSP00000410210.1:p.Asn978=
NM_001003694.1:c.2952C= NP_001003694.1:p.Asn984=
NM_004634.2:c.2934C= NP_004625.2:p.Asn978=
XM_005265449.1:c.2931C= XP_005265506.1:p.Asn977=
XM_005265450.1:c.2949C= XP_005265507.1:p.Asn983=
XM_005265451.1:c.2931C= XP_005265508.1:p.Asn977=
XM_005265452.1:c.2667C= XP_005265509.1:p.Asn889=
XM_005265453.1:c.2649C= XP_005265510.1:p.Asn883=
XM_011534101.1:c.2934C= XP_011532403.1:p.Asn978=
XM_011534102.1:c.2934C= XP_011532404.1:p.Asn978=
NM_001319049.1:c.2649C= NP_001305978.1:p.Asn883=
NM_001319050.1:c.2931C= NP_001305979.1:p.Asn977=
XM_024453741.1:c.2952C= XP_024309509.1:p.Asn984=
XM_024453742.1:c.2952C= XP_024309510.1:p.Asn984=
XM_024453743.1:c.2949C= XP_024309511.1:p.Asn983=
XM_024453744.1:c.2667C= XP_024309512.1:p.Asn889=
XR_001740257.1:n.3287C=
XR_001740258.1:n.3541C=
NM_001003694.2:c.2952C= MANE Select NP_001003694.1:p.Asn984=
NR_160918.1:n.3535C=
NM_001319049.2:c.2649C= NP_001305978.1:p.Asn883=
NM_001319050.2:c.2931C= NP_001305979.1:p.Asn977=
NM_004634.3:c.2934C= NP_004625.2:p.Asn978=