Canonical Allele Identifier: CA2580070612
Gene: BRPF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9744212dup , CM000665.2:g.9744212dup GRCh38
NC_000003.11:g.9785896dup , CM000665.1:g.9785896dup GRCh37
NC_000003.10:g.9760896dup NCBI36
NG_052955.1:g.17484dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000424362.7:c.2633-12dup ENSP00000398863.2:n.2633-12dup
ENST00000457855.2:c.2615-12dup ENSP00000410210.2:n.2615-12dup
ENST00000497565.3:n.1255-12dup
ENST00000672126.2:c.*534+311dup ENSP00000500718.1:n.*534+311dup
ENST00000672515.2:c.2633-12dup ENSP00000499951.2:n.2633-12dup
ENST00000673551.2:c.*759-12dup ENSP00000500672.1:n.*759-12dup
ENST00000682208.1:c.2615-12dup ENSP00000508123.1:n.2615-12dup
ENST00000682980.1:c.2632+311dup ENSP00000508198.1:n.2632+311dup
ENST00000683423.1:c.*123-12dup ENSP00000507659.1:n.*123-12dup
ENST00000683639.1:c.2618-12dup ENSP00000506903.1:n.2618-12dup
ENST00000683743.1:c.2618-12dup ENSP00000507469.1:n.2618-12dup
ENST00000684199.1:c.2636-12dup ENSP00000506921.1:n.2636-12dup
ENST00000684206.1:c.2614+311dup ENSP00000507148.1:n.2614+311dup
ENST00000684333.1:c.2615-12dup ENSP00000508256.1:n.2615-12dup
ENST00000684573.1:c.322-12dup
ENST00000684608.1:c.*762-12dup ENSP00000507969.1:n.*762-12dup
ENST00000383829.7:c.2636-12dup MANE Select ENSP00000373340.2:n.2636-12dup
ENST00000424362.6:c.2615-12dup ENSP00000398863.1:n.2615-12dup
ENST00000497565.2:n.1255-12dup
ENST00000672126.1:c.2835+311dup ENSP00000500718.1:n.2835+311dup
ENST00000672515.1:c.2610-12dup
ENST00000673551.1:c.*759-12dup ENSP00000500672.1:n.*759-12dup
ENST00000383829.6:c.2636-12dup ENSP00000373340.2:n.2636-12dup
ENST00000424362.5:c.2615-12dup ENSP00000398863.1:n.2615-12dup
ENST00000433861.6:c.2617+311dup ENSP00000402485.2:n.2617+311dup
ENST00000457855.1:c.2618-12dup ENSP00000410210.1:n.2618-12dup
NM_001003694.1:c.2636-12dup NP_001003694.1:n.2636-12dup
NM_004634.2:c.2618-12dup NP_004625.2:n.2618-12dup
XM_005265449.1:c.2615-12dup XP_005265506.1:n.2615-12dup
XM_005265450.1:c.2633-12dup XP_005265507.1:n.2633-12dup
XM_005265451.1:c.2615-12dup XP_005265508.1:n.2615-12dup
XM_005265452.1:c.2635+311dup XP_005265509.1:n.2635+311dup
XM_005265453.1:c.2617+311dup XP_005265510.1:n.2617+311dup
XM_011534101.1:c.2618-12dup XP_011532403.1:n.2618-12dup
XM_011534102.1:c.2618-12dup XP_011532404.1:n.2618-12dup
NM_001319049.1:c.2617+311dup NP_001305978.1:n.2617+311dup
NM_001319050.1:c.2615-12dup NP_001305979.1:n.2615-12dup
XM_024453741.1:c.2636-12dup XP_024309509.1:n.2636-12dup
XM_024453742.1:c.2636-12dup XP_024309510.1:n.2636-12dup
XM_024453743.1:c.2633-12dup XP_024309511.1:n.2633-12dup
XM_024453744.1:c.2635+311dup XP_024309512.1:n.2635+311dup
XR_001740257.1:n.3255+311dup
XR_001740258.1:n.3225-12dup
NM_001003694.2:c.2636-12dup MANE Select NP_001003694.1:n.2636-12dup
NR_160918.1:n.3219-12dup
NM_001319049.2:c.2617+311dup NP_001305978.1:n.2617+311dup
NM_001319050.2:c.2615-12dup NP_001305979.1:n.2615-12dup
NM_004634.3:c.2618-12dup NP_004625.2:n.2618-12dup