Canonical Allele Identifier: CA351705392

Gene: BRPF1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9746321C>T , CM000665.2:g.9746321C>T	GRCh38
NC_000003.11:g.9788005C>T , CM000665.1:g.9788005C>T	GRCh37
NC_000003.10:g.9763005C>T	NCBI36
NG_012106.1:g.1378C>T
NG_052955.1:g.19593C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424362.7:c.3343C>T	ENSP00000398863.2:p.Arg1115Ter
ENST00000457855.2:c.3325C>T	ENSP00000410210.2:p.Arg1109Ter
ENST00000497565.3:n.1965C>T
ENST00000672126.2:c.*960C>T	ENSP00000500718.1:n.*960C>T
ENST00000672515.2:c.3445C>T	ENSP00000499951.2:p.Arg1149Ter
ENST00000673551.2:c.*1469C>T	ENSP00000500672.1:n.*1469C>T
ENST00000682208.1:c.3427C>T	ENSP00000508123.1:p.Arg1143Ter
ENST00000682980.1:c.3058C>T	ENSP00000508198.1:p.Arg1020Ter
ENST00000683639.1:c.3430C>T	ENSP00000506903.1:p.Arg1144Ter
ENST00000683743.1:c.3328C>T	ENSP00000507469.1:p.Arg1110Ter
ENST00000683986.1:n.1122C>T
ENST00000684199.1:c.3346C>T	ENSP00000506921.1:p.Arg1116Ter
ENST00000684206.1:c.3040C>T	ENSP00000507148.1:p.Arg1014Ter
ENST00000684333.1:c.3325C>T	ENSP00000508256.1:p.Arg1109Ter
ENST00000684573.1:c.1065C>T
ENST00000684608.1:c.*1472C>T	ENSP00000507969.1:n.*1472C>T
ENST00000383829.7:c.3346C>T MANE Select	ENSP00000373340.2:p.Arg1116Ter
ENST00000424362.6:c.3325C>T	ENSP00000398863.1:p.Arg1109Ter
ENST00000497565.2:n.1965C>T
ENST00000672126.1:c.3261C>T	ENSP00000500718.1:n.3261C>T
ENST00000672515.1:c.3422C>T
ENST00000673551.1:c.*1469C>T	ENSP00000500672.1:n.*1469C>T
ENST00000383829.6:c.3346C>T	ENSP00000373340.2:p.Arg1116Ter
ENST00000424362.5:c.3325C>T	ENSP00000398863.1:p.Arg1109Ter
ENST00000433861.6:c.3043C>T	ENSP00000402485.2:p.Arg1015Ter
ENST00000457855.1:c.3328C>T	ENSP00000410210.1:p.Arg1110Ter
ENST00000497565.1:n.492C>T
NM_001003694.1:c.3346C>T	NP_001003694.1:p.Arg1116Ter
NM_004634.2:c.3328C>T	NP_004625.2:p.Arg1110Ter
XM_005265449.1:c.3427C>T	XP_005265506.1:p.Arg1143Ter
XM_005265450.1:c.3343C>T	XP_005265507.1:p.Arg1115Ter
XM_005265451.1:c.3325C>T	XP_005265508.1:p.Arg1109Ter
XM_005265452.1:c.3061C>T	XP_005265509.1:p.Arg1021Ter
XM_005265453.1:c.3043C>T	XP_005265510.1:p.Arg1015Ter
XM_011534101.1:c.3430C>T	XP_011532403.1:p.Arg1144Ter
XM_011534102.1:c.3430C>T	XP_011532404.1:p.Arg1144Ter
NM_001319049.1:c.3043C>T	NP_001305978.1:p.Arg1015Ter
NM_001319050.1:c.3325C>T	NP_001305979.1:p.Arg1109Ter
XM_024453741.1:c.3448C>T	XP_024309509.1:p.Arg1150Ter
XM_024453742.1:c.3448C>T	XP_024309510.1:p.Arg1150Ter
XM_024453743.1:c.3445C>T	XP_024309511.1:p.Arg1149Ter
XM_024453744.1:c.3163C>T	XP_024309512.1:p.Arg1055Ter
XR_001740257.1:n.3681C>T
XR_001740258.1:n.3935C>T
NM_001003694.2:c.3346C>T MANE Select	NP_001003694.1:p.Arg1116Ter
NR_160918.1:n.3929C>T
NM_001319049.2:c.3043C>T	NP_001305978.1:p.Arg1015Ter
NM_001319050.2:c.3325C>T	NP_001305979.1:p.Arg1109Ter
NM_004634.3:c.3328C>T	NP_004625.2:p.Arg1110Ter