Canonical Allele Identifier: CA351703679
Gene: BRPF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9745616C>T , CM000665.2:g.9745616C>T GRCh38
NC_000003.11:g.9787300C>T , CM000665.1:g.9787300C>T GRCh37
NC_000003.10:g.9762300C>T NCBI36
NG_012106.1:g.673C>T
NG_052955.1:g.18888C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001003694.2:c.3112C>T MANE Select NP_001003694.1:p.Arg1038Trp
ENST00000383829.7:c.3112C>T MANE Select ENSP00000373340.2:p.Arg1038Trp
NM_001003694.1:c.3112C>T NP_001003694.1:p.Arg1038Trp
NM_001319049.1:c.2809C>T NP_001305978.1:p.Arg937Trp
NM_001319049.2:c.2809C>T NP_001305978.1:p.Arg937Trp
NM_001319050.1:c.3091C>T NP_001305979.1:p.Arg1031Trp
NM_001319050.2:c.3091C>T NP_001305979.1:p.Arg1031Trp
NM_004634.2:c.3094C>T NP_004625.2:p.Arg1032Trp
NM_004634.3:c.3094C>T NP_004625.2:p.Arg1032Trp
NR_160918.1:n.3695C>T
ENST00000383829.6:c.3112C>T ENSP00000373340.2:p.Arg1038Trp
ENST00000424362.5:c.3091C>T ENSP00000398863.1:p.Arg1031Trp
ENST00000424362.6:c.3091C>T ENSP00000398863.1:p.Arg1031Trp
ENST00000424362.7:c.3109C>T ENSP00000398863.2:p.Arg1037Trp
ENST00000433861.6:c.2809C>T ENSP00000402485.2:p.Arg937Trp
ENST00000457855.1:c.3094C>T ENSP00000410210.1:p.Arg1032Trp
ENST00000457855.2:c.3091C>T ENSP00000410210.2:p.Arg1031Trp
ENST00000497565.1:n.156C>T
ENST00000497565.2:n.1731C>T
ENST00000497565.3:n.1731C>T
ENST00000672126.1:c.3027C>T ENSP00000500718.1:n.3027C>T
ENST00000672126.2:c.*726C>T ENSP00000500718.1:n.*726C>T
ENST00000672515.1:c.3086C>T
ENST00000672515.2:c.3109C>T ENSP00000499951.2:p.Arg1037Trp
ENST00000673551.1:c.*1235C>T ENSP00000500672.1:n.*1235C>T
ENST00000673551.2:c.*1235C>T ENSP00000500672.1:n.*1235C>T
ENST00000682208.1:c.3091C>T ENSP00000508123.1:p.Arg1031Trp
ENST00000682980.1:c.2824C>T ENSP00000508198.1:p.Arg942Trp
ENST00000683423.1:c.*599C>T ENSP00000507659.1:n.*599C>T
ENST00000683639.1:c.3094C>T ENSP00000506903.1:p.Arg1032Trp
ENST00000683743.1:c.3094C>T ENSP00000507469.1:p.Arg1032Trp
ENST00000683986.1:n.417C>T
ENST00000684199.1:c.3112C>T ENSP00000506921.1:p.Arg1038Trp
ENST00000684206.1:c.2806C>T ENSP00000507148.1:p.Arg936Trp
ENST00000684333.1:c.3091C>T ENSP00000508256.1:p.Arg1031Trp
ENST00000684573.1:c.831C>T
ENST00000684608.1:c.*1238C>T ENSP00000507969.1:n.*1238C>T
XM_005265449.1:c.3091C>T XP_005265506.1:p.Arg1031Trp
XM_005265450.1:c.3109C>T XP_005265507.1:p.Arg1037Trp
XM_005265451.1:c.3091C>T XP_005265508.1:p.Arg1031Trp
XM_005265452.1:c.2827C>T XP_005265509.1:p.Arg943Trp
XM_005265453.1:c.2809C>T XP_005265510.1:p.Arg937Trp
XM_011534101.1:c.3094C>T XP_011532403.1:p.Arg1032Trp
XM_011534102.1:c.3094C>T XP_011532404.1:p.Arg1032Trp
XM_024453741.1:c.3112C>T XP_024309509.1:p.Arg1038Trp
XM_024453742.1:c.3112C>T XP_024309510.1:p.Arg1038Trp
XM_024453743.1:c.3109C>T XP_024309511.1:p.Arg1037Trp
XM_024453744.1:c.2827C>T XP_024309512.1:p.Arg943Trp
XR_001740257.1:n.3447C>T
XR_001740258.1:n.3701C>T