Canonical Allele Identifier: CA432382683

Gene: BRPF1

Linked Data

• MyVariant Identifiers: chr3:g.9786768C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9745084C>T , CM000665.2:g.9745084C>T	GRCh38
NC_000003.11:g.9786768C>T , CM000665.1:g.9786768C>T	GRCh37
NC_000003.10:g.9761768C>T	NCBI36
NG_012106.1:g.141C>T
NG_052955.1:g.18356C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000424362.7:c.2994C>T	ENSP00000398863.2:p.Ser998=
ENST00000457855.2:c.2976C>T	ENSP00000410210.2:p.Ser992=
ENST00000497565.3:n.1616C>T
ENST00000672126.2:c.*611C>T	ENSP00000500718.1:n.*611C>T
ENST00000672515.2:c.2994C>T	ENSP00000499951.2:p.Ser998=
ENST00000673551.2:c.*1120C>T	ENSP00000500672.1:n.*1120C>T
ENST00000682208.1:c.2976C>T	ENSP00000508123.1:p.Ser992=
ENST00000682980.1:c.2709C>T	ENSP00000508198.1:p.Ser903=
ENST00000683423.1:c.*484C>T	ENSP00000507659.1:n.*484C>T
ENST00000683639.1:c.2979C>T	ENSP00000506903.1:p.Ser993=
ENST00000683743.1:c.2979C>T	ENSP00000507469.1:p.Ser993=
ENST00000684199.1:c.2997C>T	ENSP00000506921.1:p.Ser999=
ENST00000684206.1:c.2691C>T	ENSP00000507148.1:p.Ser897=
ENST00000684333.1:c.2976C>T	ENSP00000508256.1:p.Ser992=
ENST00000684573.1:c.716C>T
ENST00000684608.1:c.*1123C>T	ENSP00000507969.1:n.*1123C>T
ENST00000383829.7:c.2997C>T MANE Select	ENSP00000373340.2:p.Ser999=
ENST00000424362.6:c.2976C>T	ENSP00000398863.1:p.Ser992=
ENST00000497565.2:n.1616C>T
ENST00000672126.1:c.2912C>T	ENSP00000500718.1:n.2912C>T
ENST00000672515.1:c.2971C>T
ENST00000673551.1:c.*1120C>T	ENSP00000500672.1:n.*1120C>T
ENST00000383829.6:c.2997C>T	ENSP00000373340.2:p.Ser999=
ENST00000424362.5:c.2976C>T	ENSP00000398863.1:p.Ser992=
ENST00000433861.6:c.2694C>T	ENSP00000402485.2:p.Ser898=
ENST00000457855.1:c.2979C>T	ENSP00000410210.1:p.Ser993=
ENST00000497565.1:n.41C>T
NM_001003694.1:c.2997C>T	NP_001003694.1:p.Ser999=
NM_004634.2:c.2979C>T	NP_004625.2:p.Ser993=
XM_005265449.1:c.2976C>T	XP_005265506.1:p.Ser992=
XM_005265450.1:c.2994C>T	XP_005265507.1:p.Ser998=
XM_005265451.1:c.2976C>T	XP_005265508.1:p.Ser992=
XM_005265452.1:c.2712C>T	XP_005265509.1:p.Ser904=
XM_005265453.1:c.2694C>T	XP_005265510.1:p.Ser898=
XM_011534101.1:c.2979C>T	XP_011532403.1:p.Ser993=
XM_011534102.1:c.2979C>T	XP_011532404.1:p.Ser993=
NM_001319049.1:c.2694C>T	NP_001305978.1:p.Ser898=
NM_001319050.1:c.2976C>T	NP_001305979.1:p.Ser992=
XM_024453741.1:c.2997C>T	XP_024309509.1:p.Ser999=
XM_024453742.1:c.2997C>T	XP_024309510.1:p.Ser999=
XM_024453743.1:c.2994C>T	XP_024309511.1:p.Ser998=
XM_024453744.1:c.2712C>T	XP_024309512.1:p.Ser904=
XR_001740257.1:n.3332C>T
XR_001740258.1:n.3586C>T
NM_001003694.2:c.2997C>T MANE Select	NP_001003694.1:p.Ser999=
NR_160918.1:n.3580C>T
NM_001319049.2:c.2694C>T	NP_001305978.1:p.Ser898=
NM_001319050.2:c.2976C>T	NP_001305979.1:p.Ser992=
NM_004634.3:c.2979C>T	NP_004625.2:p.Ser993=