Canonical Allele Identifier: CA351702867

Gene: BRPF1

Linked Data

• gnomAD v4: 3-9745083-G-C
• MyVariant Identifiers: chr3:g.9786767G>C (hg19) ; chr3:g.9745083G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9745083G>C , CM000665.2:g.9745083G>C	GRCh38
NC_000003.11:g.9786767G>C , CM000665.1:g.9786767G>C	GRCh37
NC_000003.10:g.9761767G>C	NCBI36
NG_012106.1:g.140G>C
NG_052955.1:g.18355G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000424362.7:c.2993G>C	ENSP00000398863.2:p.Ser998Thr
ENST00000457855.2:c.2975G>C	ENSP00000410210.2:p.Ser992Thr
ENST00000497565.3:n.1615G>C
ENST00000672126.2:c.*610G>C	ENSP00000500718.1:n.*610G>C
ENST00000672515.2:c.2993G>C	ENSP00000499951.2:p.Ser998Thr
ENST00000673551.2:c.*1119G>C	ENSP00000500672.1:n.*1119G>C
ENST00000682208.1:c.2975G>C	ENSP00000508123.1:p.Ser992Thr
ENST00000682980.1:c.2708G>C	ENSP00000508198.1:p.Ser903Thr
ENST00000683423.1:c.*483G>C	ENSP00000507659.1:n.*483G>C
ENST00000683639.1:c.2978G>C	ENSP00000506903.1:p.Ser993Thr
ENST00000683743.1:c.2978G>C	ENSP00000507469.1:p.Ser993Thr
ENST00000684199.1:c.2996G>C	ENSP00000506921.1:p.Ser999Thr
ENST00000684206.1:c.2690G>C	ENSP00000507148.1:p.Ser897Thr
ENST00000684333.1:c.2975G>C	ENSP00000508256.1:p.Ser992Thr
ENST00000684573.1:c.715G>C
ENST00000684608.1:c.*1122G>C	ENSP00000507969.1:n.*1122G>C
ENST00000383829.7:c.2996G>C MANE Select	ENSP00000373340.2:p.Ser999Thr
ENST00000424362.6:c.2975G>C	ENSP00000398863.1:p.Ser992Thr
ENST00000497565.2:n.1615G>C
ENST00000672126.1:c.2911G>C	ENSP00000500718.1:n.2911G>C
ENST00000672515.1:c.2970G>C
ENST00000673551.1:c.*1119G>C	ENSP00000500672.1:n.*1119G>C
ENST00000383829.6:c.2996G>C	ENSP00000373340.2:p.Ser999Thr
ENST00000424362.5:c.2975G>C	ENSP00000398863.1:p.Ser992Thr
ENST00000433861.6:c.2693G>C	ENSP00000402485.2:p.Ser898Thr
ENST00000457855.1:c.2978G>C	ENSP00000410210.1:p.Ser993Thr
ENST00000497565.1:n.40G>C
NM_001003694.1:c.2996G>C	NP_001003694.1:p.Ser999Thr
NM_004634.2:c.2978G>C	NP_004625.2:p.Ser993Thr
XM_005265449.1:c.2975G>C	XP_005265506.1:p.Ser992Thr
XM_005265450.1:c.2993G>C	XP_005265507.1:p.Ser998Thr
XM_005265451.1:c.2975G>C	XP_005265508.1:p.Ser992Thr
XM_005265452.1:c.2711G>C	XP_005265509.1:p.Ser904Thr
XM_005265453.1:c.2693G>C	XP_005265510.1:p.Ser898Thr
XM_011534101.1:c.2978G>C	XP_011532403.1:p.Ser993Thr
XM_011534102.1:c.2978G>C	XP_011532404.1:p.Ser993Thr
NM_001319049.1:c.2693G>C	NP_001305978.1:p.Ser898Thr
NM_001319050.1:c.2975G>C	NP_001305979.1:p.Ser992Thr
XM_024453741.1:c.2996G>C	XP_024309509.1:p.Ser999Thr
XM_024453742.1:c.2996G>C	XP_024309510.1:p.Ser999Thr
XM_024453743.1:c.2993G>C	XP_024309511.1:p.Ser998Thr
XM_024453744.1:c.2711G>C	XP_024309512.1:p.Ser904Thr
XR_001740257.1:n.3331G>C
XR_001740258.1:n.3585G>C
NM_001003694.2:c.2996G>C MANE Select	NP_001003694.1:p.Ser999Thr
NR_160918.1:n.3579G>C
NM_001319049.2:c.2693G>C	NP_001305978.1:p.Ser898Thr
NM_001319050.2:c.2975G>C	NP_001305979.1:p.Ser992Thr
NM_004634.3:c.2978G>C	NP_004625.2:p.Ser993Thr