Canonical Allele Identifier: CA351702817

Gene: BRPF1

Linked Data

• MyVariant Identifiers: chr3:g.9786754C>A (hg19) ; chr3:g.9745070C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9745070C>A , CM000665.2:g.9745070C>A	GRCh38
NC_000003.11:g.9786754C>A , CM000665.1:g.9786754C>A	GRCh37
NC_000003.10:g.9761754C>A	NCBI36
NG_012106.1:g.127C>A
NG_052955.1:g.18342C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000424362.7:c.2980C>A	ENSP00000398863.2:p.Arg994Ser
ENST00000457855.2:c.2962C>A	ENSP00000410210.2:p.Arg988Ser
ENST00000497565.3:n.1602C>A
ENST00000672126.2:c.*597C>A	ENSP00000500718.1:n.*597C>A
ENST00000672515.2:c.2980C>A	ENSP00000499951.2:p.Arg994Ser
ENST00000673551.2:c.*1106C>A	ENSP00000500672.1:n.*1106C>A
ENST00000682208.1:c.2962C>A	ENSP00000508123.1:p.Arg988Ser
ENST00000682980.1:c.2695C>A	ENSP00000508198.1:p.Arg899Ser
ENST00000683423.1:c.*470C>A	ENSP00000507659.1:n.*470C>A
ENST00000683639.1:c.2965C>A	ENSP00000506903.1:p.Arg989Ser
ENST00000683743.1:c.2965C>A	ENSP00000507469.1:p.Arg989Ser
ENST00000684199.1:c.2983C>A	ENSP00000506921.1:p.Arg995Ser
ENST00000684206.1:c.2677C>A	ENSP00000507148.1:p.Arg893Ser
ENST00000684333.1:c.2962C>A	ENSP00000508256.1:p.Arg988Ser
ENST00000684573.1:c.702C>A
ENST00000684608.1:c.*1109C>A	ENSP00000507969.1:n.*1109C>A
ENST00000383829.7:c.2983C>A MANE Select	ENSP00000373340.2:p.Arg995Ser
ENST00000424362.6:c.2962C>A	ENSP00000398863.1:p.Arg988Ser
ENST00000497565.2:n.1602C>A
ENST00000672126.1:c.2898C>A	ENSP00000500718.1:n.2898C>A
ENST00000672515.1:c.2957C>A
ENST00000673551.1:c.*1106C>A	ENSP00000500672.1:n.*1106C>A
ENST00000383829.6:c.2983C>A	ENSP00000373340.2:p.Arg995Ser
ENST00000424362.5:c.2962C>A	ENSP00000398863.1:p.Arg988Ser
ENST00000433861.6:c.2680C>A	ENSP00000402485.2:p.Arg894Ser
ENST00000457855.1:c.2965C>A	ENSP00000410210.1:p.Arg989Ser
ENST00000497565.1:n.27C>A
NM_001003694.1:c.2983C>A	NP_001003694.1:p.Arg995Ser
NM_004634.2:c.2965C>A	NP_004625.2:p.Arg989Ser
XM_005265449.1:c.2962C>A	XP_005265506.1:p.Arg988Ser
XM_005265450.1:c.2980C>A	XP_005265507.1:p.Arg994Ser
XM_005265451.1:c.2962C>A	XP_005265508.1:p.Arg988Ser
XM_005265452.1:c.2698C>A	XP_005265509.1:p.Arg900Ser
XM_005265453.1:c.2680C>A	XP_005265510.1:p.Arg894Ser
XM_011534101.1:c.2965C>A	XP_011532403.1:p.Arg989Ser
XM_011534102.1:c.2965C>A	XP_011532404.1:p.Arg989Ser
NM_001319049.1:c.2680C>A	NP_001305978.1:p.Arg894Ser
NM_001319050.1:c.2962C>A	NP_001305979.1:p.Arg988Ser
XM_024453741.1:c.2983C>A	XP_024309509.1:p.Arg995Ser
XM_024453742.1:c.2983C>A	XP_024309510.1:p.Arg995Ser
XM_024453743.1:c.2980C>A	XP_024309511.1:p.Arg994Ser
XM_024453744.1:c.2698C>A	XP_024309512.1:p.Arg900Ser
XR_001740257.1:n.3318C>A
XR_001740258.1:n.3572C>A
NM_001003694.2:c.2983C>A MANE Select	NP_001003694.1:p.Arg995Ser
NR_160918.1:n.3566C>A
NM_001319049.2:c.2680C>A	NP_001305978.1:p.Arg894Ser
NM_001319050.2:c.2962C>A	NP_001305979.1:p.Arg988Ser
NM_004634.3:c.2965C>A	NP_004625.2:p.Arg989Ser