Canonical Allele Identifier: CA351685803

Gene: BRPF1

Linked Data

• ClinVar Variation Id: 559906
• ClinVar RCV Id: RCV000677700
• dbSNP Id: rs1553695017
• MyVariant Identifiers: chr3:g.9780987C>T (hg19) ; chr3:g.9739303C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9739303C>T , CM000665.2:g.9739303C>T	GRCh38
NC_000003.11:g.9780987C>T , CM000665.1:g.9780987C>T	GRCh37
NC_000003.10:g.9755987C>T	NCBI36
NG_052955.1:g.12575C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420291.3:c.904C>T	ENSP00000416728.3:p.Gln302Ter
ENST00000424362.7:c.904C>T	ENSP00000398863.2:p.Gln302Ter
ENST00000426583.2:c.904C>T	ENSP00000404235.2:p.Gln302Ter
ENST00000457855.2:c.904C>T	ENSP00000410210.2:p.Gln302Ter
ENST00000672126.2:c.904C>T	ENSP00000500718.1:p.Gln302Ter
ENST00000672515.2:c.904C>T	ENSP00000499951.2:p.Gln302Ter
ENST00000673551.2:c.904C>T	ENSP00000500672.1:p.Gln302Ter
ENST00000682208.1:c.904C>T	ENSP00000508123.1:p.Gln302Ter
ENST00000682980.1:c.904C>T	ENSP00000508198.1:p.Gln302Ter
ENST00000683423.1:c.904C>T	ENSP00000507659.1:p.Gln302Ter
ENST00000683639.1:c.904C>T	ENSP00000506903.1:p.Gln302Ter
ENST00000683743.1:c.904C>T	ENSP00000507469.1:p.Gln302Ter
ENST00000684199.1:c.904C>T	ENSP00000506921.1:p.Gln302Ter
ENST00000684206.1:c.904C>T	ENSP00000507148.1:p.Gln302Ter
ENST00000684223.1:c.904C>T	ENSP00000506789.1:p.Gln302Ter
ENST00000684333.1:c.904C>T	ENSP00000508256.1:p.Gln302Ter
ENST00000684608.1:c.904C>T	ENSP00000507969.1:p.Gln302Ter
ENST00000383829.7:c.904C>T MANE Select	ENSP00000373340.2:p.Gln302Ter
ENST00000424362.6:c.904C>T	ENSP00000398863.1:p.Gln302Ter
ENST00000672126.1:c.904C>T	ENSP00000500718.1:p.Gln302Ter
ENST00000672515.1:c.896C>T
ENST00000673551.1:c.904C>T	ENSP00000500672.1:p.Gln302Ter
ENST00000383829.6:c.904C>T	ENSP00000373340.2:p.Gln302Ter
ENST00000424362.5:c.904C>T	ENSP00000398863.1:p.Gln302Ter
ENST00000433861.6:c.904C>T	ENSP00000402485.2:p.Gln302Ter
ENST00000457855.1:c.904C>T	ENSP00000410210.1:p.Gln302Ter
NM_001003694.1:c.904C>T	NP_001003694.1:p.Gln302Ter
NM_004634.2:c.904C>T	NP_004625.2:p.Gln302Ter
XM_005265449.1:c.904C>T	XP_005265506.1:p.Gln302Ter
XM_005265450.1:c.904C>T	XP_005265507.1:p.Gln302Ter
XM_005265451.1:c.904C>T	XP_005265508.1:p.Gln302Ter
XM_005265452.1:c.904C>T	XP_005265509.1:p.Gln302Ter
XM_005265453.1:c.904C>T	XP_005265510.1:p.Gln302Ter
XM_005265454.1:c.904C>T	XP_005265511.1:p.Gln302Ter
XM_011534101.1:c.904C>T	XP_011532403.1:p.Gln302Ter
XM_011534102.1:c.904C>T	XP_011532404.1:p.Gln302Ter
NM_001319049.1:c.904C>T	NP_001305978.1:p.Gln302Ter
NM_001319050.1:c.904C>T	NP_001305979.1:p.Gln302Ter
XM_024453741.1:c.904C>T	XP_024309509.1:p.Gln302Ter
XM_024453742.1:c.904C>T	XP_024309510.1:p.Gln302Ter
XM_024453743.1:c.904C>T	XP_024309511.1:p.Gln302Ter
XM_024453744.1:c.904C>T	XP_024309512.1:p.Gln302Ter
XR_001740257.1:n.1324C>T
XR_001740258.1:n.1324C>T
NM_001003694.2:c.904C>T MANE Select	NP_001003694.1:p.Gln302Ter
NR_160918.1:n.1318C>T
NM_001319049.2:c.904C>T	NP_001305978.1:p.Gln302Ter
NM_001319050.2:c.904C>T	NP_001305979.1:p.Gln302Ter
NM_004634.3:c.904C>T	NP_004625.2:p.Gln302Ter