Canonical Allele Identifier: CA432382631

Gene: BRPF1

Linked Data

• gnomAD v4: 3-9745072-T-C
• MyVariant Identifiers: chr3:g.9786756T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9745072T>C , CM000665.2:g.9745072T>C	GRCh38
NC_000003.11:g.9786756T>C , CM000665.1:g.9786756T>C	GRCh37
NC_000003.10:g.9761756T>C	NCBI36
NG_012106.1:g.129T>C
NG_052955.1:g.18344T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000424362.7:c.2982T>C	ENSP00000398863.2:p.Arg994=
ENST00000457855.2:c.2964T>C	ENSP00000410210.2:p.Arg988=
ENST00000497565.3:n.1604T>C
ENST00000672126.2:c.*599T>C	ENSP00000500718.1:n.*599T>C
ENST00000672515.2:c.2982T>C	ENSP00000499951.2:p.Arg994=
ENST00000673551.2:c.*1108T>C	ENSP00000500672.1:n.*1108T>C
ENST00000682208.1:c.2964T>C	ENSP00000508123.1:p.Arg988=
ENST00000682980.1:c.2697T>C	ENSP00000508198.1:p.Arg899=
ENST00000683423.1:c.*472T>C	ENSP00000507659.1:n.*472T>C
ENST00000683639.1:c.2967T>C	ENSP00000506903.1:p.Arg989=
ENST00000683743.1:c.2967T>C	ENSP00000507469.1:p.Arg989=
ENST00000684199.1:c.2985T>C	ENSP00000506921.1:p.Arg995=
ENST00000684206.1:c.2679T>C	ENSP00000507148.1:p.Arg893=
ENST00000684333.1:c.2964T>C	ENSP00000508256.1:p.Arg988=
ENST00000684573.1:c.704T>C
ENST00000684608.1:c.*1111T>C	ENSP00000507969.1:n.*1111T>C
ENST00000383829.7:c.2985T>C MANE Select	ENSP00000373340.2:p.Arg995=
ENST00000424362.6:c.2964T>C	ENSP00000398863.1:p.Arg988=
ENST00000497565.2:n.1604T>C
ENST00000672126.1:c.2900T>C	ENSP00000500718.1:n.2900T>C
ENST00000672515.1:c.2959T>C
ENST00000673551.1:c.*1108T>C	ENSP00000500672.1:n.*1108T>C
ENST00000383829.6:c.2985T>C	ENSP00000373340.2:p.Arg995=
ENST00000424362.5:c.2964T>C	ENSP00000398863.1:p.Arg988=
ENST00000433861.6:c.2682T>C	ENSP00000402485.2:p.Arg894=
ENST00000457855.1:c.2967T>C	ENSP00000410210.1:p.Arg989=
ENST00000497565.1:n.29T>C
NM_001003694.1:c.2985T>C	NP_001003694.1:p.Arg995=
NM_004634.2:c.2967T>C	NP_004625.2:p.Arg989=
XM_005265449.1:c.2964T>C	XP_005265506.1:p.Arg988=
XM_005265450.1:c.2982T>C	XP_005265507.1:p.Arg994=
XM_005265451.1:c.2964T>C	XP_005265508.1:p.Arg988=
XM_005265452.1:c.2700T>C	XP_005265509.1:p.Arg900=
XM_005265453.1:c.2682T>C	XP_005265510.1:p.Arg894=
XM_011534101.1:c.2967T>C	XP_011532403.1:p.Arg989=
XM_011534102.1:c.2967T>C	XP_011532404.1:p.Arg989=
NM_001319049.1:c.2682T>C	NP_001305978.1:p.Arg894=
NM_001319050.1:c.2964T>C	NP_001305979.1:p.Arg988=
XM_024453741.1:c.2985T>C	XP_024309509.1:p.Arg995=
XM_024453742.1:c.2985T>C	XP_024309510.1:p.Arg995=
XM_024453743.1:c.2982T>C	XP_024309511.1:p.Arg994=
XM_024453744.1:c.2700T>C	XP_024309512.1:p.Arg900=
XR_001740257.1:n.3320T>C
XR_001740258.1:n.3574T>C
NM_001003694.2:c.2985T>C MANE Select	NP_001003694.1:p.Arg995=
NR_160918.1:n.3568T>C
NM_001319049.2:c.2682T>C	NP_001305978.1:p.Arg894=
NM_001319050.2:c.2964T>C	NP_001305979.1:p.Arg988=
NM_004634.3:c.2967T>C	NP_004625.2:p.Arg989=