Canonical Allele Identifier: CA351702860

Gene: BRPF1

Linked Data

• MyVariant Identifiers: chr3:g.9786765C>G (hg19) ; chr3:g.9745081C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9745081C>G , CM000665.2:g.9745081C>G	GRCh38
NC_000003.11:g.9786765C>G , CM000665.1:g.9786765C>G	GRCh37
NC_000003.10:g.9761765C>G	NCBI36
NG_012106.1:g.138C>G
NG_052955.1:g.18353C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000424362.7:c.2991C>G	ENSP00000398863.2:p.Cys997Trp
ENST00000457855.2:c.2973C>G	ENSP00000410210.2:p.Cys991Trp
ENST00000497565.3:n.1613C>G
ENST00000672126.2:c.*608C>G	ENSP00000500718.1:n.*608C>G
ENST00000672515.2:c.2991C>G	ENSP00000499951.2:p.Cys997Trp
ENST00000673551.2:c.*1117C>G	ENSP00000500672.1:n.*1117C>G
ENST00000682208.1:c.2973C>G	ENSP00000508123.1:p.Cys991Trp
ENST00000682980.1:c.2706C>G	ENSP00000508198.1:p.Cys902Trp
ENST00000683423.1:c.*481C>G	ENSP00000507659.1:n.*481C>G
ENST00000683639.1:c.2976C>G	ENSP00000506903.1:p.Cys992Trp
ENST00000683743.1:c.2976C>G	ENSP00000507469.1:p.Cys992Trp
ENST00000684199.1:c.2994C>G	ENSP00000506921.1:p.Cys998Trp
ENST00000684206.1:c.2688C>G	ENSP00000507148.1:p.Cys896Trp
ENST00000684333.1:c.2973C>G	ENSP00000508256.1:p.Cys991Trp
ENST00000684573.1:c.713C>G
ENST00000684608.1:c.*1120C>G	ENSP00000507969.1:n.*1120C>G
ENST00000383829.7:c.2994C>G MANE Select	ENSP00000373340.2:p.Cys998Trp
ENST00000424362.6:c.2973C>G	ENSP00000398863.1:p.Cys991Trp
ENST00000497565.2:n.1613C>G
ENST00000672126.1:c.2909C>G	ENSP00000500718.1:n.2909C>G
ENST00000672515.1:c.2968C>G
ENST00000673551.1:c.*1117C>G	ENSP00000500672.1:n.*1117C>G
ENST00000383829.6:c.2994C>G	ENSP00000373340.2:p.Cys998Trp
ENST00000424362.5:c.2973C>G	ENSP00000398863.1:p.Cys991Trp
ENST00000433861.6:c.2691C>G	ENSP00000402485.2:p.Cys897Trp
ENST00000457855.1:c.2976C>G	ENSP00000410210.1:p.Cys992Trp
ENST00000497565.1:n.38C>G
NM_001003694.1:c.2994C>G	NP_001003694.1:p.Cys998Trp
NM_004634.2:c.2976C>G	NP_004625.2:p.Cys992Trp
XM_005265449.1:c.2973C>G	XP_005265506.1:p.Cys991Trp
XM_005265450.1:c.2991C>G	XP_005265507.1:p.Cys997Trp
XM_005265451.1:c.2973C>G	XP_005265508.1:p.Cys991Trp
XM_005265452.1:c.2709C>G	XP_005265509.1:p.Cys903Trp
XM_005265453.1:c.2691C>G	XP_005265510.1:p.Cys897Trp
XM_011534101.1:c.2976C>G	XP_011532403.1:p.Cys992Trp
XM_011534102.1:c.2976C>G	XP_011532404.1:p.Cys992Trp
NM_001319049.1:c.2691C>G	NP_001305978.1:p.Cys897Trp
NM_001319050.1:c.2973C>G	NP_001305979.1:p.Cys991Trp
XM_024453741.1:c.2994C>G	XP_024309509.1:p.Cys998Trp
XM_024453742.1:c.2994C>G	XP_024309510.1:p.Cys998Trp
XM_024453743.1:c.2991C>G	XP_024309511.1:p.Cys997Trp
XM_024453744.1:c.2709C>G	XP_024309512.1:p.Cys903Trp
XR_001740257.1:n.3329C>G
XR_001740258.1:n.3583C>G
NM_001003694.2:c.2994C>G MANE Select	NP_001003694.1:p.Cys998Trp
NR_160918.1:n.3577C>G
NM_001319049.2:c.2691C>G	NP_001305978.1:p.Cys897Trp
NM_001319050.2:c.2973C>G	NP_001305979.1:p.Cys991Trp
NM_004634.3:c.2976C>G	NP_004625.2:p.Cys992Trp