Canonical Allele Identifier: CA351702839

Gene: BRPF1

Linked Data

• MyVariant Identifiers: chr3:g.9786760G>C (hg19) ; chr3:g.9745076G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9745076G>C , CM000665.2:g.9745076G>C	GRCh38
NC_000003.11:g.9786760G>C , CM000665.1:g.9786760G>C	GRCh37
NC_000003.10:g.9761760G>C	NCBI36
NG_012106.1:g.133G>C
NG_052955.1:g.18348G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000424362.7:c.2986G>C	ENSP00000398863.2:p.Asp996His
ENST00000457855.2:c.2968G>C	ENSP00000410210.2:p.Asp990His
ENST00000497565.3:n.1608G>C
ENST00000672126.2:c.*603G>C	ENSP00000500718.1:n.*603G>C
ENST00000672515.2:c.2986G>C	ENSP00000499951.2:p.Asp996His
ENST00000673551.2:c.*1112G>C	ENSP00000500672.1:n.*1112G>C
ENST00000682208.1:c.2968G>C	ENSP00000508123.1:p.Asp990His
ENST00000682980.1:c.2701G>C	ENSP00000508198.1:p.Asp901His
ENST00000683423.1:c.*476G>C	ENSP00000507659.1:n.*476G>C
ENST00000683639.1:c.2971G>C	ENSP00000506903.1:p.Asp991His
ENST00000683743.1:c.2971G>C	ENSP00000507469.1:p.Asp991His
ENST00000684199.1:c.2989G>C	ENSP00000506921.1:p.Asp997His
ENST00000684206.1:c.2683G>C	ENSP00000507148.1:p.Asp895His
ENST00000684333.1:c.2968G>C	ENSP00000508256.1:p.Asp990His
ENST00000684573.1:c.708G>C
ENST00000684608.1:c.*1115G>C	ENSP00000507969.1:n.*1115G>C
ENST00000383829.7:c.2989G>C MANE Select	ENSP00000373340.2:p.Asp997His
ENST00000424362.6:c.2968G>C	ENSP00000398863.1:p.Asp990His
ENST00000497565.2:n.1608G>C
ENST00000672126.1:c.2904G>C	ENSP00000500718.1:n.2904G>C
ENST00000672515.1:c.2963G>C
ENST00000673551.1:c.*1112G>C	ENSP00000500672.1:n.*1112G>C
ENST00000383829.6:c.2989G>C	ENSP00000373340.2:p.Asp997His
ENST00000424362.5:c.2968G>C	ENSP00000398863.1:p.Asp990His
ENST00000433861.6:c.2686G>C	ENSP00000402485.2:p.Asp896His
ENST00000457855.1:c.2971G>C	ENSP00000410210.1:p.Asp991His
ENST00000497565.1:n.33G>C
NM_001003694.1:c.2989G>C	NP_001003694.1:p.Asp997His
NM_004634.2:c.2971G>C	NP_004625.2:p.Asp991His
XM_005265449.1:c.2968G>C	XP_005265506.1:p.Asp990His
XM_005265450.1:c.2986G>C	XP_005265507.1:p.Asp996His
XM_005265451.1:c.2968G>C	XP_005265508.1:p.Asp990His
XM_005265452.1:c.2704G>C	XP_005265509.1:p.Asp902His
XM_005265453.1:c.2686G>C	XP_005265510.1:p.Asp896His
XM_011534101.1:c.2971G>C	XP_011532403.1:p.Asp991His
XM_011534102.1:c.2971G>C	XP_011532404.1:p.Asp991His
NM_001319049.1:c.2686G>C	NP_001305978.1:p.Asp896His
NM_001319050.1:c.2968G>C	NP_001305979.1:p.Asp990His
XM_024453741.1:c.2989G>C	XP_024309509.1:p.Asp997His
XM_024453742.1:c.2989G>C	XP_024309510.1:p.Asp997His
XM_024453743.1:c.2986G>C	XP_024309511.1:p.Asp996His
XM_024453744.1:c.2704G>C	XP_024309512.1:p.Asp902His
XR_001740257.1:n.3324G>C
XR_001740258.1:n.3578G>C
NM_001003694.2:c.2989G>C MANE Select	NP_001003694.1:p.Asp997His
NR_160918.1:n.3572G>C
NM_001319049.2:c.2686G>C	NP_001305978.1:p.Asp896His
NM_001319050.2:c.2968G>C	NP_001305979.1:p.Asp990His
NM_004634.3:c.2971G>C	NP_004625.2:p.Asp991His