Canonical Allele Identifier: CA2646557768

Gene: BRDT

Linked Data

• gnomAD v4: 1-91962951-G-GTATGTCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91962952_91962959dup , CM000663.2:g.91962952_91962959dup	GRCh38
NC_000001.10:g.92428509_92428516dup , CM000663.1:g.92428509_92428516dup	GRCh37
NC_000001.9:g.92201097_92201104dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000399546.7:c.192+6_192+13dup MANE Select	ENSP00000387822.3:n.192+6_192+13dup
ENST00000426141.6:c.192+6_192+13dup	ENSP00000404969.1:n.192+6_192+13dup
ENST00000448194.6:c.192+6_192+13dup	ENSP00000410587.2:n.192+6_192+13dup
ENST00000470955.6:c.192+6_192+13dup	ENSP00000506247.1:n.192+6_192+13dup
ENST00000680091.1:c.234+6_234+13dup	ENSP00000506227.1:n.234+6_234+13dup
ENST00000680541.1:c.-21-5194_-21-5187dup	ENSP00000505035.1:n.-21-5194_-21-5187dup
ENST00000362005.7:c.192+6_192+13dup	ENSP00000354568.3:n.192+6_192+13dup
ENST00000370389.6:c.-27-1675_-27-1668dup	ENSP00000359416.2:n.-27-1675_-27-1668dup
ENST00000394530.7:c.192+6_192+13dup	ENSP00000378038.3:n.192+6_192+13dup
ENST00000399546.6:c.192+6_192+13dup	ENSP00000387822.2:n.192+6_192+13dup
ENST00000402388.1:c.192+6_192+13dup	ENSP00000384051.1:n.192+6_192+13dup
ENST00000423434.5:c.192+6_192+13dup	ENSP00000396351.1:n.192+6_192+13dup
ENST00000426141.5:c.192+6_192+13dup	ENSP00000404969.1:n.192+6_192+13dup
ENST00000427104.5:c.192+6_192+13dup	ENSP00000400002.1:n.192+6_192+13dup
ENST00000440509.5:c.192+6_192+13dup	ENSP00000416714.1:n.192+6_192+13dup
ENST00000448194.5:c.192+6_192+13dup	ENSP00000410587.1:n.192+6_192+13dup
ENST00000450792.5:c.192+6_192+13dup	ENSP00000414349.1:n.192+6_192+13dup
ENST00000548992.5:c.192+6_192+13dup	ENSP00000447394.1:n.192+6_192+13dup
ENST00000552654.1:c.-28+6_-28+13dup	ENSP00000446599.1:n.-28+6_-28+13dup
NM_001242805.2:c.192+6_192+13dup	NP_001229734.2:n.192+6_192+13dup
NM_001242806.2:c.192+6_192+13dup	NP_001229735.2:n.192+6_192+13dup
NM_001242807.2:c.192+6_192+13dup	NP_001229736.2:n.192+6_192+13dup
NM_001242808.2:c.192+6_192+13dup	NP_001229737.2:n.192+6_192+13dup
NM_001242810.2:c.-27-1675_-27-1668dup	NP_001229739.2:n.-27-1675_-27-1668dup
NM_001726.4:c.192+6_192+13dup	NP_001717.3:n.192+6_192+13dup
NM_207189.3:c.192+6_192+13dup	NP_997072.2:n.192+6_192+13dup
XM_006710853.2:c.192+6_192+13dup	XP_006710916.1:n.192+6_192+13dup
XM_006710854.2:c.192+6_192+13dup	XP_006710917.1:n.192+6_192+13dup
XM_006710855.2:c.192+6_192+13dup	XP_006710918.1:n.192+6_192+13dup
XM_006710856.2:c.192+6_192+13dup	XP_006710919.1:n.192+6_192+13dup
XM_006710857.2:c.192+6_192+13dup	XP_006710920.1:n.192+6_192+13dup
XM_011542032.1:c.192+6_192+13dup	XP_011540334.1:n.192+6_192+13dup
XM_011542033.1:c.192+6_192+13dup	XP_011540335.1:n.192+6_192+13dup
XM_011542034.1:c.192+6_192+13dup	XP_011540336.1:n.192+6_192+13dup
XM_011542035.1:c.192+6_192+13dup	XP_011540337.1:n.192+6_192+13dup
XM_011542036.1:c.192+6_192+13dup	XP_011540338.1:n.192+6_192+13dup
XM_006710853.4:c.192+6_192+13dup	XP_006710916.1:n.192+6_192+13dup
XM_006710854.4:c.192+6_192+13dup	XP_006710917.1:n.192+6_192+13dup
XM_006710855.4:c.192+6_192+13dup	XP_006710918.1:n.192+6_192+13dup
XM_006710856.4:c.192+6_192+13dup	XP_006710919.1:n.192+6_192+13dup
XM_006710857.4:c.192+6_192+13dup	XP_006710920.1:n.192+6_192+13dup
XM_011542032.3:c.192+6_192+13dup	XP_011540334.1:n.192+6_192+13dup
XM_011542033.3:c.192+6_192+13dup	XP_011540335.1:n.192+6_192+13dup
XM_011542034.3:c.192+6_192+13dup	XP_011540336.1:n.192+6_192+13dup
XM_011542035.3:c.192+6_192+13dup	XP_011540337.1:n.192+6_192+13dup
XM_011542036.3:c.192+6_192+13dup	XP_011540338.1:n.192+6_192+13dup
NM_207189.4:c.192+6_192+13dup MANE Select	NP_997072.2:n.192+6_192+13dup