Canonical Allele Identifier: CA404484134

Gene: BRD4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15264452G>T , CM000681.2:g.15264452G>T	GRCh38
NC_000019.9:g.15375263G>T , CM000681.1:g.15375263G>T	GRCh37
NC_000019.8:g.15236263G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001379291.1:c.1164C>A MANE Select	NP_001366220.1:p.His388Gln
ENST00000679869.1:c.1164C>A MANE Select	ENSP00000506350.1:p.His388Gln
NM_001330384.1:c.1164C>A	NP_001317313.1:p.His388Gln
NM_001330384.2:c.1164C>A	NP_001317313.1:p.His388Gln
NM_001379292.1:c.1164C>A	NP_001366221.1:p.His388Gln
NM_014299.2:c.1164C>A	NP_055114.1:p.His388Gln
NM_014299.3:c.1164C>A	NP_055114.1:p.His388Gln
NM_058243.2:c.1164C>A	NP_490597.1:p.His388Gln
NM_058243.3:c.1164C>A	NP_490597.1:p.His388Gln
ENST00000263377.6:c.1164C>A	ENSP00000263377.1:p.His388Gln
ENST00000360016.9:c.1164C>A	ENSP00000353112.4:p.His388Gln
ENST00000371835.8:c.1164C>A	ENSP00000360901.3:p.His388Gln
ENST00000594841.5:c.1164C>A	ENSP00000470481.1:p.His388Gln
ENST00000678800.1:n.169C>A
XM_011527854.1:c.1164C>A	XP_011526156.1:p.His388Gln
XM_011527854.2:c.1164C>A	XP_011526156.1:p.His388Gln
XM_011527855.1:c.1164C>A	XP_011526157.1:p.His388Gln
XM_011527856.1:c.1164C>A	XP_011526158.1:p.His388Gln
XM_011527856.3:c.1164C>A	XP_011526158.1:p.His388Gln